Whole exome sequencing of a family with MAIS
收藏NIAID Data Ecosystem2026-03-13 收录
下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA867577
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资源简介：
This study aimed to find out the genetic variations related to a Chinese family with mild androgen insensitivity syndrome (MAIS) that usually shows the phenotype of azoospermia resulting in male infertility.
创建时间：
2022-08-09
