A rare deleterious missense mutation in the AXIN2 gene in Chinese women with polycystic ovary syndrome

A rare deleterious missense mutation in the AXIN2 gene in Chinese women with polycystic ovary syndrome

Background Polycystic ovary syndrome (PCOS) is an endocrine disorders and characterized by polycystic ovary morphology and oligomenorrhea, affecting fertility and health condition of female around the world. The causative factors of PCOS are complex, and genetic structure remains a long-standing med...

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Bibliographic Details
Main Authors: Ying Zhang, Yu Chen, Fa-Ying Liu, Jing-Wen Fu, Xian-Xian Liu, Jun Tan, Ou-Ping Huang, Yang Zou
Format: Article
Language:English
Published: Taylor & Francis Group 2025-12-01
Series:Gynecological Endocrinology
Subjects:
Polycystic ovary syndrome
Chinese
mutation
AXIN2
Wnt/β-catenin signaling pathway
Online Access:https://www.tandfonline.com/doi/10.1080/09513590.2025.2463545
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https://www.tandfonline.com/doi/10.1080/09513590.2025.2463545

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