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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Hum Genome Var
मुख्य लेखकों: Akizawa, Yoshika, Yamamoto, Toshiyuki, Tamura, Kazuo, Kanno, Toshiyuki, Takahashi, Nobuko, Ohki, Takeshi, Omori, Teppei, Tokushige, Katsutoshi, Yamamoto, Masakazu, Saito, Kayoko
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Nature Publishing Group UK 2018
विषय:
Data Report
ऑनलाइन पहुंच: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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