Novel variants in STAG2 and PKD1 associate with multiple congenital malformations and autosomal dominant polycystic kidney disease in a Chinese family-1
收藏NIAID Data Ecosystem2026-05-10 收录
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https://data.mendeley.com/datasets/sx3c492n72
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资源简介：
Trio whole-exome sequencing (Trio-WES) was performed on a Chinese family to investigate the genetic etiology of the proband’s multiple congenital malformations and familial PKD.
创建时间：
2025-09-10
