A Homozygous Splicing Mutation in PDE2A in a Family With Atypical Rett Syndrome

Saved in:
Bibliographic Details
Published inMovement disorders Vol. 35; no. 5; pp. 896 - 899
Main Authors Haidar, Zahraa, Jalkh, Nadine, Corbani, Sandra, Abou‐Ghoch, Joelle, Fawaz, Ali, Mehawej, Cybel, Chouery, Eliane
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.05.2020
Wiley Subscription Services, Inc
Subjects
Cyclic Nucleotide Phosphodiesterases, Type 2
Homozygote
Humans
Movement disorders
Mutation - genetics
Phenotype
Rett syndrome
Rett Syndrome - genetics
Splicing
Online AccessGet full text

Cover

More Information
Bibliography:Nothing to report.
Relevant conflicts of interests/financial disclosures
This work (samples collection, analysis, and interpretation of data) was supported by grants from the Research Council of Saint Joseph University, Beirut, Lebanon (FM333). The authors did not receive any personal funding.
Funding agencies
SourceType-Other Sources-1
ObjectType-Article-2
content type line 63
ObjectType-Correspondence-1
ISSN:0885-3185
1531-8257
DOI:10.1002/mds.28023