Articles with "ercc6 variant" as a keyword



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A novel heterozygous ERCC6 variant identified in a Chinese family with non‐syndromic primary ovarian insufficiency

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Published in 2022 at "Molecular Genetics & Genomic Medicine"

DOI: 10.1002/mgg3.2040

Abstract: Premature ovarian insufficiency (POI) is a clinical syndrome occurring in women before 40 with decreased ovarian function. Up to 25% of POI cases result from genetic factors that remain largely unknown. The Excision repair cross‐complementing,… read more here.

Keywords: novel heterozygous; ovarian insufficiency; ercc6 variant;