MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversions.

MYH associated polyposis is a hereditary syndrome responsible for early colorectal cancer with a distinct genetic pathway from the Familial Adenomatous Polyposis or the Hereditary Non Polyposis Colorectal Cancer syndrome. We have studied a family with three members bearing a biallelic mutation in MY...

Полное описание

Библиографические подробности
Главные авторы: Lefevre, J, Colas, C, Coulet, F, Bonilla, C, Mourra, N, Flejou, J, Tiret, E, Bodmer, W, Soubrier, F, Parc, Y
Формат: Journal article
Язык:English
Опубликовано: 2010