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MOESM8 of De novo variants in exomes of congenital heart disease patients identify risk genes and pathways

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DataCite Commons2024-02-08 更新2024-07-28 收录
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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
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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.
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figshare
创建时间:
2020-01-16
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