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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Hum Genome Var
Päätekijät: Akizawa, Yoshika, Yamamoto, Toshiyuki, Tamura, Kazuo, Kanno, Toshiyuki, Takahashi, Nobuko, Ohki, Takeshi, Omori, Teppei, Tokushige, Katsutoshi, Yamamoto, Masakazu, Saito, Kayoko
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group UK 2018
Aiheet:
Data Report
Linkit: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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