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colorectal cancer, hereditary nonpolyposis, type 2
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MLH1
The interacting domains of three MutL heterodimers in man: hMLH1 interacts with 36 homologous amino acid residues within hMLH3, hPMS1 and hPMS2
The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer
Clinicopathological relevance of the association between gastrointestinal and sebaceous neoplasms: the Muir-Torre syndrome.
Cancer Gene Census
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MLH1
Somatic tumors
colorectal, endometrial, ovarian, CNS tumours
Tumor types germline
colorectal, endometrial, ovarian, CNS
Cancer Syndrom
hereditary non-polyposis colorectal cancer, Turcot syndrome
Translocation partner
Name
E.coli MutL homolog gene
Chromosome banding
3p21.3
Cancer molecular gen.
Rec
Mutation type
D, Mis, N, F, S
Other syndrome disease
Definition
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Pathways
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Clinical Trials
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External
Mesalamine for Colorectal Cancer Prevention Program in Lynch Syndrome (MesaCAPP)