A novel MLH1 mutation in a Japanese family with Lynch syndrome associated with small bowel cancer

Lynch syndrome is a genetic disorder related to cancer predisposition, including colorectal cancer, endometrial cancer, and ovarian cancer. Germline mutations in mismatch repair genes, including MLH1, MSH2, MSH6, and PMS2, are responsible for this condition. Cancer tissue specimens resected from sma...

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Detalhes bibliográficos
Publicado no:Hum Genome Var
Main Authors: Akizawa, Yoshika, Yamamoto, Toshiyuki, Tamura, Kazuo, Kanno, Toshiyuki, Takahashi, Nobuko, Ohki, Takeshi, Omori, Teppei, Tokushige, Katsutoshi, Yamamoto, Masakazu, Saito, Kayoko
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2018
Assuntos:
Data Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6013486/
https://ncbi.nlm.nih.gov/pubmed/30083359
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41439-018-0013-y
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