Additional file 1 of Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study
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Additional file 1: Table S1. Detail phenotypes of individuals with ASD, Table S2. Known ASD/NDD gene panels, Table S3. Known mtDNA pathogenic variants associated with hearing loss/Deafness at greater than 2% heteroplasmy, Table S4. Candidate dominant variants in Novel genes/regions associated with ASD.
创建时间:
2024-08-14



