Empty follicle syndrome caused by non-cleavable mutation of ZP2 furin cleavage site
收藏NIAID Data Ecosystem2026-03-12 收录
下载链接：
https://www.ncbi.nlm.nih.gov/sra/SRP264750
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资源简介：
A rare damaging variant in the CFCS domain of ZP2 was identified by whole-exome sequencing in three unrelated families with clinical manifestations suggestive of GEFS.
创建时间：
2021-01-01
