MOESM1 of De novo variants in exomes of congenital heart disease patients identify risk genes and pathways
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https://springernature.figshare.com/articles/dataset/MOESM1_of_De_novo_variants_in_exomes_of_congenital_heart_disease_patients_identify_risk_genes_and_pathways/11626479
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资源简介：
Additional file 1: Cases and controls: Table S1. Ethnicity and sex distributions of all CHD cases and controls, Table S2. Filtered de novo mutations in cases, Table S3. Filtered de novo mutations in controls.
附加文件1：病例与对照：表S1. 所有冠心病（CHD）病例与对照的种族及性别分布，表S2. 病例中经筛选的新发突变，表S3. 对照中经筛选的新发突变。
提供机构：
Itan, Yuval; Tristani-Firouzi, Martin; Gelb, Bruce; Sevim Bayrak, Cigdem; Zhang, Peng
创建时间：
2020-01-16
