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Paper Details

Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.
Am J Hum Genet
321
2013
AFF2, ASD, ASD risk genes, Autism Spectrum Disorder, CAPRIN1, CHARGE syndrome, CHD7, FMR1, KCNQ2, NRXN1, SCN2A, VIP, autism spectrum disorder, epilepsy, fragile X syndrome, social-cognitive deficits
Author NameAffiliation
Yong-Hui JiangDuke University School of Medicine
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Datasets

Release 1.2