Výsledky vyhledávání - "MutS Homolog 2 Protein/deficiency"

A case of Muir-Torre syndrome associated with mucinous hepatic cholangiocarcinoma and a novel germline mutation of the MSH2 gene

Autor: M. Vernez, O. Gugerli, N. Halkic, P. Hutter, Hanifa Bouzourene, C. Monnerat

Publikováno v: Familial Cancer, vol. 6, no. 1, pp. 141-145

Muir-Torre syndrome (MTS) is a rare cancer-predisposing syndrome that is autosomal dominantly inherited and characterized by the development of sebaceous skin lesions (adenomas, epitheliomas, basaliomas and carcinomas). These lesions are typically as

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e5938883bf5826766a13f0d7e2e2601
https://pubmed.ncbi.nlm.nih.gov/17051350

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