MOESM8 of De novo variants in exomes of congenital heart disease patients identify risk genes and pathways
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https://figshare.com/articles/dataset/MOESM8_of_De_novo_variants_in_exomes_of_congenital_heart_disease_patients_identify_risk_genes_and_pathways/11626533
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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.
创建时间：
2020-01-15
