KLB mutations in congenital hypogonadotropic hypogonadism
收藏NIAID Data Ecosystem2026-03-10 收录
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资源简介：
To test if patients with congenital hypogonadotropic hypogonadism harbor mutations in FGF21 and KLB (encoding the co-receptor of FGF21)EGA study EGAS00001002568
创建时间：
2017-08-04
