Clinicopathological features of Lynch syndrome pedigrees with MSH2 c.351G>A gene variant

Clinicopathological features of Lynch syndrome pedigrees with MSH2 c.351G>A gene variant

Abstract Background Lynch syndrome (LS) is an autosomal‐dominant disorder that increases the risk of many cancers. To identify novel or rare pathogenic variants of MMR genes associated with LS, especially in Chinese pedigrees. Methods One four‐generation Chinese Han family from northeast China with...

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Bibliographic Details
Main Authors: Shuai Zhang, Guanyu Fu, Gongping Sun, Yuanxin Tang, Jin Meng, Zhigang Wang, Rongjun Su, Wei Liu, Xiaoxia Li
Format: Article
Language:English
Published: Wiley 2025-01-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
Chinese family
clinicopathological features
Lynch syndrome
MSH2 gene variant
Online Access:https://doi.org/10.1002/mgg3.2506
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