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

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 these diso...

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Detalles Bibliográficos
Autores principales: Bitar, Tania, Hleihel, Walid, Marouillat, Sylviane, Vonwill, Sandrine, Vuillaume, Marie‐Laure, Soufia, Michel, Vourc'h, Patrick, Laumonnier, Frederic, Andres, Christian R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687626/
https://www.ncbi.nlm.nih.gov/pubmed/31254375
http://dx.doi.org/10.1002/mgg3.786

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687626/
https://www.ncbi.nlm.nih.gov/pubmed/31254375
http://dx.doi.org/10.1002/mgg3.786

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