Functional Characterization of a Missense Variant of MLH1 Identified in Lynch Syndrome Pedigree

Lynch syndrome (LS) is the most common hereditary colorectal cancer (CRCs) inherited in an autosomal-dominant manner. Here, we reported a multigeneration Chinese family clinically diagnosed with LS according to the Amsterdam II criteria. To identify the underlying causative gene for LS in this famil...

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Pubblicato in:Dis Markers
Autori principali: Zaib, Tahir, Zhang, Chunhui, Saleem, Komal, Xu, Lidan, Qin, Qian, Wang, Yusi, Ji, Wei, Khan, Hanif, Yu, Hanfei, Zhu, Siqi, Gao, Wei, Huang, Yun, Jia, Xueyuan, Wu, Jie, Song, Hongtao, Zhang, Yanqiao, Sun, Wenjing, Fu, Songbin
Natura: Artigo
Lingua:Inglês
Pubblicazione: Hindawi 2020
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7008259/
https://ncbi.nlm.nih.gov/pubmed/32076465
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/8360841
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