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Article

Association analysis between HFM1 variation and primary ovarian insufficiency in Chinese women.

Clinical genetics - 1 May 2016

Pu D, Wang C, Cao J, Shen Y, Jiang H, Liu J, Wu B L, Zhang W, Wu J

Abstract excerpt

HFM1 is a meiosis-specific gene and expressed in germ-line tissues. More recently, evidence has indicated that variations in HFM1 gene could be causative for primary ovarian insufficiency (POI), also known as premature ovarian failure. The aim of this study was to investigate the association between HFM1 gene variants and sporadic POI in Chinese women. A total of 138 POI patients and 316 healthy controls (matched...

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Identifiers

PMID: 26679638
DOI: 10.1111/cge.12718

Genes

HFM1

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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