Identification of rare copy number variations reveals PJA2, APCS, SYNPO, and TAC1 as novel candidate genes in Autism Spectrum Disorders

Identification of rare copy number variations reveals PJA2, APCS, SYNPO, and TAC1 as novel candidate genes in Autism Spectrum Disorders

Abstract Background There is a strong evidence for genetic factors as the main causes of Autism Spectrum Disorders (ASD). To date, hundreds of genes have been identified either by copy number variations (CNVs) and/or single nucleotide variations. However, despite all the findings, the genetics of th...

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Bibliographic Details
Main Authors: Tania Bitar, Walid Hleihel, Sylviane Marouillat, Sandrine Vonwill, Marie‐Laure Vuillaume, Michel Soufia, Patrick Vourc'h, Frederic Laumonnier, Christian R. Andres
Format: Article
Language:English
Published: Wiley 2019-08-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
APCS
Autism Spectrum Disorders
CGHarray
copy number variations
PJA2
SYNPO
Online Access:https://doi.org/10.1002/mgg3.786

Internet

https://doi.org/10.1002/mgg3.786

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