hMSH2 is the most commonly mutated MMR gene in a cohort of Greek HNPCC patients

Germline mutations in genes encoding proteins involved in DNA mismatch repair are responsible for the autosomal dominantly inherited cancer predisposition syndrome hereditary nonpolyposis colorectal cancer (HNPCC). We describe here analysis of hMLH1 and hMSH2 in nine Greek families referred to our c...

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Detalhes bibliográficos
Main Authors: Apessos, A, Mihalatos, M, Danielidis, I, Kallimanis, G, Agnantis, N J, Triantafillidis, J K, Fountzilas, G, Kosmidis, P A, Razis, E, Georgoulias, V A, Nasioulas, G
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2005
Assuntos:
Genetics and Genomics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2361846/
https://ncbi.nlm.nih.gov/pubmed/15655560
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.bjc.6602260
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