Lack of association of WNT5A mutations with Müllerian duct abnormalities.

doi:10.1016/j.rbmo.2012.10.015

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Article

Lack of association of WNT5A mutations with Müllerian duct abnormalities.

Reproductive biomedicine online - 1 Feb 2013

Wu Keliang, Chang Xinyue, Wei Deying, Xu Chengyan, Qin Yingying, Chen Zi-Jiang

Abstract excerpt

The aim of this study was to determine if mutations in WNT5A contribute to the aetiology of Müllerian duct abnormalities (MDA) in 189 Chinese women. Three novel single-nucleotide polymorphisms (SNP; IVS2 - 115G >A, IVS4 + 66T >A, IVS4 + 102G >T) in introns 2 and 4 as well as one known SNP (rs62620048) in exon 6 were detected, but no causal mutations were observed. The results suggested that mutations in WNT5A may...

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PMID: 23265959
DOI: 10.1016/j.rbmo.2012.10.015

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

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