首页> 外文期刊>The journal of clinical endocrinology and metabolism >A Biallelic Mutation in the Homologous Recombination Repair Gene SPIDR Is Associated With Human Gonadal Dysgenesis
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A Biallelic Mutation in the Homologous Recombination Repair Gene SPIDR Is Associated With Human Gonadal Dysgenesis

机译:同源重组修复基因SPIDR中的双等位基因突变与人类性腺发育不全相关。

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AbstractContext:Primary ovarian insufficiency (POI) is caused by ovarian follicle depletion or follicle dysfunction, characterized by amenorrhea with elevated gonadotropin levels. The disorder presents as absence of normal progression of puberty.
机译:摘要背景:原发性卵巢功能不全(POI)是由卵巢卵泡消耗或卵泡功能障碍引起的,其特征为闭经性腺激素水平升高。这种疾病表现为青春期没有正常进展。

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