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Article

Novel missense mutation in WNT6 in 100 couples with unexplained recurrent miscarriage.

Human reproduction (Oxford, England) - 1 Apr 2015

Zhang Yimei, Li Guangyu, Fan Yuanyuan, Cui Yuqian, Huang Sexin, Ma Jinlong, Yan Junhao, Chen Zi-Jiang

Abstract excerpt

STUDY QUESTION: Do mutations and/or polymorphisms in coding sequences in Wingless-Type MMTV Integration Site Family, Member 6 (WNT6) play a role in unexplained recurrent miscarriage (unexplained RM) in Chinese couples? SUMMARY ANSWER: We found four mutations in the coding sequences of WNT6 which appear to exist in a small proportion of Chinese women with unexplained RM. WHAT IS KNOWN ALREADY: WNT6 has been proved...

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Source

Identifiers

PMID: 25750203
DOI: 10.1093/humrep/dev028

Genes

WNT6

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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