Additional file 1 of Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study
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https://springernature.figshare.com/articles/dataset/Additional_file_1_of_Genomic_architecture_of_autism_spectrum_disorder_in_Qatar_The_BARAKA-Qatar_Study/26624452/1
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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.
补充材料1：表S1 自闭症谱系障碍（Autism Spectrum Disorder, ASD）患者的详细表型信息；表S2 已知自闭症谱系障碍/神经发育障碍（Neurodevelopmental Disorder, NDD）基因检测面板；表S3 已知与听力损失/耳聋相关、异质性水平高于2%的线粒体DNA（mitochondrial DNA, mtDNA）致病性变异；表S4 与自闭症谱系障碍相关的新基因/区域中的候选显性变异
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figshare
创建时间：
2024-08-14
