DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function

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Bibliographic Details
Published inJournal of medical genetics Vol. 41; no. 3; pp. e22 - 22
Main Authors Lockhart, P J, Lincoln, S, Hulihan, M, Kachergus, J, Wilkes, K, Bisceglio, G, Mash, D C, Farrer, M J
Format Journal Article
LanguageEnglish
Published England BMJ Publishing Group Ltd 01.03.2004
BMJ Publishing Group LTD
BMJ Group
Subjects
Acetylcysteine - analogs & derivatives
Acetylcysteine - pharmacology
Adolescent
Adult
Age of Onset
Amino Acid Sequence
Animals
Cell Line
DNA Mutational Analysis
early onset parkinsonism
Electronic Letter
EO-PD
Family medical history
Female
Genes, Recessive - genetics
genetics
Humans
Intracellular Signaling Peptides and Proteins
Male
Middle Aged
Molecular Sequence Data
Mutation
Mutation - genetics
Oncogene Proteins - chemistry
Oncogene Proteins - genetics
Oncogene Proteins - metabolism
open reading frame
ORF
PARK7
Parkinson's disease
Parkinsonian Disorders - genetics
Patients
Protein Deglycase DJ-1
protein instability
Proteins
RNA, Messenger - genetics
RNA, Messenger - metabolism
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More Information
Bibliography:Correspondence to:
 Dr P J Lockhart
 Birdsall Building, Mayo Clinic Jacksonville, 4500 San Pablo Road, Jacksonville, FL, USA, 32224; caseyandpaul@hotmail.com
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href:jmedgenet-41-e22.pdf
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PMID:14985393
SourceType-Other Sources-1
ObjectType-Article-2
content type line 63
ObjectType-Correspondence-1
ISSN:0022-2593
1468-6244
1468-6244
DOI:10.1136/jmg.2003.011106