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 autoso...

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محفوظ في:

التفاصيل البيبلوغرافية
المؤلف الرئيسي:	Vijay Gupta (209146) (author)
مؤلفون آخرون:	Afif Ben-Mahmoud (13913550) (author), Bonsu Ku (85687) (author), Dinesh Velayutham (5444072) (author), Zainab Jan (17306614) (author), Abdi Yousef Aden (19459540) (author), Ahmad Kubbar (17306620) (author), Fouad Alshaban (6176771) (author), Lawrence W. Stanton (6707191) (author), Puthen Veettil Jithesh (12040358) (author), Lawrence C. Layman (13913559) (author), Hyung-Goo Kim (728597) (author)
منشور في:	2023
الموضوعات:	Biological sciences Genetics Biomedical and clinical sciences Clinical sciences Neurosciences exome sequencing autism intellectual disability digenic TRPC4 SCFD2
الوسوم:	إضافة وسم لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!

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

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