MOESM8 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/MOESM8_of_De_novo_variants_in_exomes_of_congenital_heart_disease_patients_identify_risk_genes_and_pathways/11626533/1
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资源简介：
Additional file 8: Table S39. Functional effects of DNMs on 23 plausible candidate genes in cases, Table S40. De novo mutations in validation set, Table S41. Human CHD genes, Table S42. Mouse CHD genes.
提供机构：
Itan, Yuval; Tristani-Firouzi, Martin; Gelb, Bruce; Sevim Bayrak, Cigdem; Zhang, Peng
创建时间：
2020-01-16
