Tryptophan hydroxylase gene 218A/C polymorphism is not associated with depressed suicide

Abnormalities in functioning of the central serotonergic system are believed to be involved in the pathogenesis of depressive illness and suicidal behaviour. Recently, polymorphism in the tryptophan hydroxylase (TPH) gene has been studied for association with aggression, anger-related traits and sui...

Full description

Saved in:
Bibliographic Details
Published inThe international journal of neuropsychopharmacology Vol. 3; no. 3; pp. 215 - 220
Main Authors Du, Lisheng, Faludi, Gabor, Palkovits, Miklos, Bakish, David, Hrdina, Pavel D.
Format Journal Article
LanguageEnglish
Published Cambridge, UK Cambridge University Press 01.09.2000
Oxford University Press
Subjects
Online AccessGet full text
ISSN1461-1457
1469-5111
1469-5111
DOI10.1017/S1461145700001954

Cover

Loading…
Abstract Abnormalities in functioning of the central serotonergic system are believed to be involved in the pathogenesis of depressive illness and suicidal behaviour. Recently, polymorphism in the tryptophan hydroxylase (TPH) gene has been studied for association with aggression, anger-related traits and suicidal behaviour, but the results are inconclusive. The present investigation was to determine whether there are differences in genotype and allele distribution of the TPH gene 218A/C polymorphism in post-mortem brain samples from 35 depressed suicide victims and 84 control subjects of the same ethnic background. A functional polymorphism in the promoter region of 5-HT transporter gene was also re-examined in this increased sample size. No significant difference in TPH gene 218A/C polymorphism between controls and depressed suicide victims was detected. This may suggest that the TPH gene has no significant effect on suicidality in depressed subjects. In a previous study on a smaller sample we found the frequency of the long allele of 5-HT transporter gene to be higher in depressed suicide victims. In this increased sample size, both the genotype and alleles of the 5-HT transporter gene were significantly associated with completed suicide. The frequency of the L/L genotype in depressed suicide victims was almost double of that found in control group (48.6 vs. 26.2%). The odds ratio for the L allele associated with depressed suicide was 2.1 (95% CI, 1.2–3.7). The relatively small sample size does not exclude the possibility of false-positive results and the finding needs replication.
AbstractList Abnormalities in functioning of the central serotonergic system are believed to be involved in the pathogenesis of depressive illness and suicidal behaviour. Recently, polymorphism in the tryptophan hydroxylase (TPH) gene has been studied for association with aggression, anger-related traits and suicidal behaviour, but the results are inconclusive. The present investigation was to determine whether there are differences in genotype and allele distribution of the TPH gene 218A/C polymorphism in post-mortem brain samples from 35 depressed suicide victims and 84 control subjects of the same ethnic background. A functional polymorphism in the promoter region of 5-HT transporter gene was also re-examined in this increased sample size. No significant difference in TPH gene 218A/C polymorphism between controls and depressed suicide victims was detected. This may suggest that the TPH gene has no significant effect on suicidality in depressed subjects. In a previous study on a smaller sample we found the frequency of the long allele of 5-HT transporter gene to be higher in depressed suicide victims. In this increased sample size, both the genotype and alleles of the 5-HT transporter gene were significantly associated with completed suicide. The frequency of the L/L genotype in depressed suicide victims was almost double of that found in control group (48.6 vs. 26.2%). The odds ratio for the L allele associated with depressed suicide was 2.1 (95% CI, 1.2–3.7). The relatively small sample size does not exclude the possibility of false-positive results and the finding needs replication.
Abnormalities in functioning of the central serotonergic system are believed to be involved in the pathogenesis of depressive illness and suicidal behaviour. Recently, polymorphism in the tryptophan hydroxylase (TPH) gene has been studied for association with aggression, anger-related traits and suicidal behaviour, but the results are inconclusive. The present investigation was to determine whether there are differences in genotype and allele distribution of the TPH gene 218A/C polymorphism in post-mortem brain samples from 35 depressed suicide victims and 84 control subjects of the same ethnic background. A functional polymorphism in the promoter region of 5-HT transporter gene was also re-examined in this increased sample size. No significant difference in TPH gene 218A/C polymorphism between controls and depressed suicide victims was detected. This may suggest that the TPH gene has no significant effect on suicidality in depressed subjects. In a previous study on a smaller sample we found the frequency of the long allele of 5-HT transporter gene to be higher in depressed suicide victims. In this increased sample size, both the genotype and alleles of the 5-HT transporter gene were significantly associated with completed suicide. The frequency of the L/L genotype in depressed suicide victims was almost double of that found in control group (48.6 vs. 26.2%). The odds ratio for the L allele associated with depressed suicide was 2.1 (95% CI, 1.2–3.7). The relatively small sample size does not exclude the possibility of false-positive results and the finding needs replication.
Abnormalities in functioning of the central serotonergic system are believed to be involved in the pathogenesis of depressive illness and suicidal behaviour. Recently, polymorphism in the tryptophan hydroxylase (TPH) gene has been studied for association with aggression, anger-related traits and suicidal behaviour, but the results are inconclusive. The present investigation was to determine whether there are differences in genotype and allele distribution of the TPH gene 218A/C polymorphism in post-mortem brain samples from 35 depressed suicide victims and 84 control subjects of the same ethnic background. A functional polymorphism in the promoter region of 5-HT transporter gene was also re-examined in this increased sample size. No significant difference in TPH gene 218A/C polymorphism between controls and depressed suicide victims was detected. This may suggest that the TPH gene has no significant effect on suicidality in depressed subjects. In a previous study on a smaller sample we found the frequency of the long allele of 5-HT transporter gene to be higher in depressed suicide victims. In this increased sample size, both the genotype and alleles of the 5-HT transporter gene were significantly associated with completed suicide. The frequency of the L/L genotype in depressed suicide victims was almost double of that found in control group (48.6 vs. 26.2%). The odds ratio for the L allele associated with depressed suicide was 2.1 (95% CI, 1.2-3.7). The relatively small sample size does not exclude the possibility of false-positive results and the finding needs replication.Abnormalities in functioning of the central serotonergic system are believed to be involved in the pathogenesis of depressive illness and suicidal behaviour. Recently, polymorphism in the tryptophan hydroxylase (TPH) gene has been studied for association with aggression, anger-related traits and suicidal behaviour, but the results are inconclusive. The present investigation was to determine whether there are differences in genotype and allele distribution of the TPH gene 218A/C polymorphism in post-mortem brain samples from 35 depressed suicide victims and 84 control subjects of the same ethnic background. A functional polymorphism in the promoter region of 5-HT transporter gene was also re-examined in this increased sample size. No significant difference in TPH gene 218A/C polymorphism between controls and depressed suicide victims was detected. This may suggest that the TPH gene has no significant effect on suicidality in depressed subjects. In a previous study on a smaller sample we found the frequency of the long allele of 5-HT transporter gene to be higher in depressed suicide victims. In this increased sample size, both the genotype and alleles of the 5-HT transporter gene were significantly associated with completed suicide. The frequency of the L/L genotype in depressed suicide victims was almost double of that found in control group (48.6 vs. 26.2%). The odds ratio for the L allele associated with depressed suicide was 2.1 (95% CI, 1.2-3.7). The relatively small sample size does not exclude the possibility of false-positive results and the finding needs replication.
ArticleNumber S1461145700001954
Author Bakish, David
Hrdina, Pavel D.
Du, Lisheng
Palkovits, Miklos
Faludi, Gabor
Author_xml – sequence: 1
  givenname: Lisheng
  surname: Du
  fullname: Du, Lisheng
  organization: Institute of Mental Health Research at Royal Ottawa Hospital and University of Ottawa, Ontario, Canada
– sequence: 2
  givenname: Gabor
  surname: Faludi
  fullname: Faludi, Gabor
  organization: Semmelweis Medical University, Budapest, Hungary
– sequence: 3
  givenname: Miklos
  surname: Palkovits
  fullname: Palkovits, Miklos
  organization: Semmelweis Medical University, Budapest, Hungary
– sequence: 4
  givenname: David
  surname: Bakish
  fullname: Bakish, David
  organization: Institute of Mental Health Research at Royal Ottawa Hospital and University of Ottawa, Ontario, Canada
– sequence: 5
  givenname: Pavel D.
  surname: Hrdina
  fullname: Hrdina, Pavel D.
  organization: Institute of Mental Health Research at Royal Ottawa Hospital and University of Ottawa, Ontario, Canada
BackLink https://www.ncbi.nlm.nih.gov/pubmed/11343598$$D View this record in MEDLINE/PubMed
BookMark eNqNkUtvFSEUgImpsQ_9AW4MiRsXTssZGAaWzY2PJk26aE3cEQaYXpqZYQQmOv9e6r3WpEZTNsDh-w4HzjE6mMLkEHoN5BQItGfXwDgAa1pSBsiGPUNHJSSrBgAOfq2huj8_RMcp3RFSs4byF-gQgDLaSHGEvt7Edc5h3uoJb1cbw4910MnhWzc5XIM4P9vgOQzrGOK89WnEPuEpZKxTCsbr7Cz-7vMWWzdHl1LZpsUbb91L9LzXQ3Kv9vMJ-vLxw83mc3V59elic35ZGdZArih3knDCgWomGPSs5Z3stTCSWduIXhDS9h2lVFqtNdOmp9YY62rXM13XHT1B73Z55xi-LS5lNfpk3DDoyYUlKRC0YZJTLgv69hF6F5Y4leoUBS6FkIUt1Js9tXSjs2qOftRxVb__rADtDjAxpBRdr4zPOvsw5aj9oICo--6ov7pTTHhkPiT_j_N-54RlfhJO91fosYve3ro_j_y39RMGnaud
CitedBy_id crossref_primary_10_1002_ajmg_b_30788
crossref_primary_10_1111_j_1601_183X_2005_00171_x
crossref_primary_10_1016_j_comppsych_2015_05_002
crossref_primary_10_1038_sj_mp_4001890
crossref_primary_10_1192_bjp_181_4_350
crossref_primary_10_1016_j_chc_2006_05_010
crossref_primary_10_1016_j_jagp_2013_06_001
crossref_primary_10_1016_j_pnpbp_2018_08_007
crossref_primary_10_1027__0227_5910_22_2_54
crossref_primary_10_1016_S0165_0327_00_00274_3
crossref_primary_10_1002_ajmg_b_30271
crossref_primary_10_1016_j_psychres_2008_10_032
crossref_primary_10_17116_jnevro202012010169
crossref_primary_10_1590_S0047_20852009000200011
crossref_primary_10_1016_S0006_3223_02_01748_1
crossref_primary_10_1038_sj_mp_4001803
crossref_primary_10_1177_0002764202250661
crossref_primary_10_1002_ajmg_b_20015
crossref_primary_10_1186_1471_244X_14_196
crossref_primary_10_1038_sj_mp_4001128
crossref_primary_10_3389_fpsyt_2022_932135
crossref_primary_10_1016_j_euroneuro_2013_03_013
crossref_primary_10_1016_S0022_3956_03_00048_7
crossref_primary_10_1007_s00439_005_0113_x
crossref_primary_10_1027__0227_5910_22_2_61
crossref_primary_10_3389_fnins_2017_00074
crossref_primary_10_1002_ajmg_10518
crossref_primary_10_1016_j_forsciint_2004_10_001
crossref_primary_10_17816_ecogen5422_43
ContentType Journal Article
Copyright 2000 Collegium Internationale Neuropsychopharmacologicum
2000 Collegium Internationale Neuropsychopharmacologicum 2000
2000 Collegium Internationale Neuropsychopharmacologicum.
Copyright_xml – notice: 2000 Collegium Internationale Neuropsychopharmacologicum
– notice: 2000 Collegium Internationale Neuropsychopharmacologicum 2000
– notice: 2000 Collegium Internationale Neuropsychopharmacologicum.
DBID AAYXX
CITATION
NPM
3V.
7X7
7XB
88E
88G
8AO
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BENPR
CCPQU
DWQXO
FYUFA
GHDGH
GNUQQ
K9.
M0S
M1P
M2M
PHGZM
PHGZT
PIMPY
PJZUB
PKEHL
PPXIY
PQEST
PQQKQ
PQUKI
PRINS
PSYQQ
Q9U
7X8
DOI 10.1017/S1461145700001954
DatabaseName CrossRef
PubMed
ProQuest Central (Corporate)
ProQuest Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
Psychology Database (Alumni)
ProQuest Pharma Collection
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
ProQuest Central
ProQuest One Community College
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
ProQuest Health & Medical Complete (Alumni)
ProQuest Health & Medical Collection
Medical Database
Psychology Database
ProQuest Central Premium
ProQuest One Academic (New)
Publicly Available Content Database
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
ProQuest One Psychology
ProQuest Central Basic
MEDLINE - Academic
DatabaseTitle CrossRef
PubMed
Publicly Available Content Database
ProQuest One Psychology
ProQuest Central Student
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Pharma Collection
ProQuest Central China
ProQuest Central
ProQuest Health & Medical Research Collection
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
Health & Medical Research Collection
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest Central Basic
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Psychology Journals (Alumni)
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest Psychology Journals
ProQuest One Academic UKI Edition
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList

MEDLINE - Academic
PubMed
Publicly Available Content Database
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Pharmacy, Therapeutics, & Pharmacology
EISSN 1469-5111
EndPage 220
ExternalDocumentID 11343598
10_1017_S1461145700001954
10.1017/S1461145700001954
Genre Journal Article
GroupedDBID ---
-E.
.FH
0E1
0R~
0VX
123
29J
3V.
4.4
53G
5VS
74X
74Y
7X7
7~V
88E
8AO
8FI
8FJ
8R4
8R5
AAFWJ
AAMVS
AAOGV
AAPPN
AAPXW
AAVAP
ABITZ
ABIVO
ABKKG
ABMYL
ABPTD
ABQLI
ABUWG
ABXVV
ACGFS
ACIMK
ADBBV
ADHZD
ADRAZ
AEMTW
AENEX
AENZO
AFFVI
AFKRA
AFPKN
AFULF
AFUTZ
AHMBA
AJ7
ALMA_UNASSIGNED_HOLDINGS
ALUQC
AOIJS
ARABE
AVWKF
AZQEC
BAWUL
BAYMD
BCNDV
BENPR
BPHCQ
BTTYL
BVXVI
C0O
CAG
CCPQU
CIDKT
COF
CS3
DC4
DIK
DU5
DWQXO
EBS
EJD
EMOBN
FYUFA
GNUQQ
GROUPED_DOAJ
HG-
HMCUK
HST
HYE
HZ~
I.6
IAO
IHR
I~P
J36
J38
J3A
KQ8
KSI
L98
LW7
M-V
M1P
M2M
M48
ML0
M~E
O9-
OAWHX
OJQWA
OJZSN
OK1
P2P
PEELM
PQQKQ
PROAC
PSQYO
PSYQQ
Q2X
RHF
RIG
ROL
ROX
RPM
RR0
S6-
S70
TJX
TOX
TUQ
UKHRP
UU6
WQ3
WXU
WXY
WYP
ABEJV
ABGNP
ABVKB
ALIPV
AMNDL
AAYXX
CITATION
H13
ITC
PHGZM
PHGZT
PIMPY
NPM
7XB
8FK
K9.
PJZUB
PKEHL
PPXIY
PQEST
PQUKI
PRINS
Q9U
7X8
PUEGO
ID FETCH-LOGICAL-c451t-36e9060613a4841f476b9fa8c94dd58f8007fb3339daaa4acf3dccde2ef4a22b3
IEDL.DBID M48
ISSN 1461-1457
1469-5111
IngestDate Fri Sep 05 05:12:30 EDT 2025
Fri Jul 25 21:57:26 EDT 2025
Wed Feb 19 01:26:17 EST 2025
Tue Jul 01 01:04:00 EDT 2025
Thu Apr 24 23:02:49 EDT 2025
Tue Feb 04 08:58:38 EST 2025
Wed Mar 13 05:53:15 EDT 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 3
Keywords serotonin
polymorphism
Tryptophan hydroxylase gene
genetics
depression
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c451t-36e9060613a4841f476b9fa8c94dd58f8007fb3339daaa4acf3dccde2ef4a22b3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.1017/S1461145700001954
PMID 11343598
PQID 3169889835
PQPubID 43629
PageCount 6
ParticipantIDs proquest_miscellaneous_1835496369
proquest_journals_3169889835
pubmed_primary_11343598
crossref_citationtrail_10_1017_S1461145700001954
crossref_primary_10_1017_S1461145700001954
oup_primary_10_1017_S1461145700001954
cambridge_journals_10_1017_S1461145700001954
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2000-09-01
PublicationDateYYYYMMDD 2000-09-01
PublicationDate_xml – month: 09
  year: 2000
  text: 2000-09-01
  day: 01
PublicationDecade 2000
PublicationPlace Cambridge, UK
PublicationPlace_xml – name: Cambridge, UK
– name: England
– name: Oxford
PublicationTitle The international journal of neuropsychopharmacology
PublicationTitleAlternate Int. J. Neuropsychopharm
PublicationYear 2000
Publisher Cambridge University Press
Oxford University Press
Publisher_xml – name: Cambridge University Press
– name: Oxford University Press
SSID ssj0024536
Score 1.7391608
Snippet Abnormalities in functioning of the central serotonergic system are believed to be involved in the pathogenesis of depressive illness and suicidal behaviour....
Abnormalities in functioning of the central serotonergic system are believed to be involved in the pathogenesis of depressive illness and suicidal behaviour....
SourceID proquest
pubmed
crossref
oup
cambridge
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 215
SubjectTerms Genotype & phenotype
Polymorphism
Suicidal behavior
Suicides & suicide attempts
SummonAdditionalLinks – databaseName: ProQuest Central
  dbid: BENPR
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3dT-MwDLeO8cILAo6PcTuUk4AHtIp2SdPkCe0QCCGBJjSkvU1pkopJox10e-h_f_GarUJI0z02dfoRO7bl2D8DnMtIKYt5YTo0ScBSQQMlszBgTCLgGQ3tEoHv6Zk_vLLHUTzyAbfSp1WudOJSUZtCY4z8mkZcCiGdw3Az-wiwaxServoWGluw7VSwiFuw_ffuefDSoO3F1NcXRUHE4mR1romg0TiIY8sAt8R-AA26whcr9aXy7ZsDujRE93uw6z1I0q9Zvg8_bH4Al4MagrrqkmFTUVV2ySUZNODU1U8YDT-rGYIJqJy8VQaTWJz_bImTI0ucIe5f35JZMa3eC8eASflOJiXJizlRno3WEAzdEp9B6y7LxURPjD2E1_u74e1D4LsrBJrF0Tyg3MqQozlXTLAoYwlPZaaElsyYWGTOk0yylFIqjVKKKZ1Ro7WxPZsx1eul9AhaeZHbEyDUcMGcZyCY5YwbpEZYPSVlIhMlVBu665Ud-z1Sjuv8smT8jRFtCFeLP9YeqRwbZkw3TblaT5nVMB2biC8cR_-HrrPiefPVjRy24c_6ttuTeNCiclss3J9hNM1pNi7bcFzLSvO2iDJETTzd_PBfsFMX_WM2Wwda88-F_e3cn3l65mX8H7l9-ow
  priority: 102
  providerName: ProQuest
Title Tryptophan hydroxylase gene 218A/C polymorphism is not associated with depressed suicide
URI https://www.cambridge.org/core/product/identifier/S1461145700001954/type/journal_article
https://www.ncbi.nlm.nih.gov/pubmed/11343598
https://www.proquest.com/docview/3169889835
https://www.proquest.com/docview/1835496369
Volume 3
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV3dT9swED_x8bKXiQ3YyljlSRsPqBlJfXXsh2liCIQ2gcrWSn2rnNgRlUrSNa20_PfzNUkzBELjMco5H_c75y723e8APqpAa0t5YbFvQg8jyT2tEt9DVER4xn27YuC7uhaXQ_w-6o02oG5vVSkwf_TXjvpJDefTz39-F1_dhP9SsQSd_KLe1AESU_uq_g03Yds5JkFGfoWyod7r8arYKPBIvN7kfOwS_1It3HNZ98rgHkSjK690sQMvq3CSnZb4v4INm76Go37JR1102KApr8o77Ij1G6bqYhdGg3kxI2YBnbLbwlBGiwumLXNGZZnzyqcnZ2yWTYu7zKExye_YJGdptmC6wtQaRuu4rEqndYf5chJPjN2D4cX54OzSq1oteDH2goXHhVW-IN-uUWKQYCgilWgZKzSmJxMXVoZJxDlXRmuNOk64iWNjuzZB3e1GfB-20iy1b4FxIyS6MEGiFSgMSRPHnlYqVKGWugWdtWbHNd7jMtksHD8AogV-rfxxXNGWU_eM6VNDjtdDZiVnx1PCnxyi_yN3WGPePDV3RialclFsCz6sT7sJSrsuOrXZ0r0ZLa25z5xQLXhT2kpzt4AjUSgePE8n7-BFyQhAqW6HsLWYL-17FxstojZshqOwDdvfzq_7P93RjxvZXs2Cvz6OAvs
linkProvider Scholars Portal
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1fT9swED8xeNhepv1fB9s8afAwNSKJHcd-mCbGQGVAVU1F6ltwbEerBEkhraZ8qX3G-ZqkEUKq9sJjHNtJfOe7y_nudwCfZaCUxbgw7ZvYY6mgnpKZ7zEmEfCM-naJwHc-5IML9nMSTTbgb5sLg2GVrUxcCmpTaPSR79OASyGkMxi-zW48rBqFp6ttCY2aLU5t9cf9spVfT344-u6G4fHR-HDgNVUFPM2iYO5RbqXPUY0pJliQsZinMlNCS2ZMJDJnQcVZSimVRinFlM6o0drY0GZMhWFK3byPYMuZGdLtoq3vR8PRrw7dL6JNPlPgBSyK23NUBKnGRmxbOtQl1h_o0BzuaMU7mXb3DN6l4jt-Bk8bi5Uc1Cz2HDZs_gL2RjXkddUn4y6Dq-yTPTLqwLCrlzAZ31YzBC9QOfldGQyacfa6JY5vLXGK_2D_kMyKq-q6cASfltdkWpK8mBPVsI01BF3FpInYdZflYqqnxr6CiwdZ99ewmRe5fQuEGi6Ys0QEs5xxg70Rxk9JGctYCdWD_mplk2ZPlkkdzxYn9wjRA79d_EQ3yOhYoONq3ZAvqyGzGhZkXeddR9H_6bfT0rx7647ve_BpddvJADzYUbktFu7L0HvnJCmXPXhT80r3tIAiq4p36yf_CI8H4_Oz5OxkeLoNT2rAAYyk24HN-e3Cvnem1zz90PA7gcuH3mL_APszOMQ
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Tryptophan+hydroxylase+gene+218A%2FC+polymorphism+is+not+associated+with+depressed+suicide&rft.jtitle=The+international+journal+of+neuropsychopharmacology&rft.au=Du%2C+Lisheng&rft.au=Faludi%2C+Gabor&rft.au=Palkovits%2C+Miklos&rft.au=Bakish%2C+David&rft.date=2000-09-01&rft.pub=Cambridge+University+Press&rft.issn=1461-1457&rft.eissn=1469-5111&rft.volume=3&rft.issue=3&rft.spage=215&rft.epage=220&rft_id=info:doi/10.1017%2FS1461145700001954&rft.externalDocID=10_1017_S1461145700001954
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1461-1457&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1461-1457&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1461-1457&client=summon