SPATA22 mutations causing NOA and POI
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA770429
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资源简介：
Bi-allelic variants of SPATA22 were firstly reported in both familial and sporadic patients with POI. The same variant revealed that SPATA22 variant might induce the loss of germ cells by impaired meiotic synapsis.
创建时间：
2021-10-11
