Identification of two novel autism genes, TRPC4 and SCFD2, in Qatar simplex families through exome sequencing

This study investigated the genetic underpinnings of autism spectrum disorder (ASD) in a Middle Eastern cohort in Qatar using exome sequencing. The study identified six candidate autism genes in independent simplex families, including both four known and two novel autosomal dominant and autosomal re...

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Detalles Bibliográficos
Autores principales: Gupta, Vijay, Ben-Mahmoud, Afif, Ku, Bonsu, Velayutham, Dinesh, Jan, Zainab, Yousef Aden, Abdi, Kubbar, Ahmad, Alshaban, Fouad, Stanton, Lawrence W., Jithesh, Puthen Veettil, Layman, Lawrence C., Kim, Hyung-Goo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Psychiatry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644705/
https://www.ncbi.nlm.nih.gov/pubmed/38025430
http://dx.doi.org/10.3389/fpsyt.2023.1251884

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644705/
https://www.ncbi.nlm.nih.gov/pubmed/38025430
http://dx.doi.org/10.3389/fpsyt.2023.1251884

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