The Mutational Spectrum of Lynch Syndrome in Cyprus

Lynch syndrome is the most common form of hereditary colorectal cancer and is caused by germline mutations in the mismatch repair (MMR) genes MLH1, MSH2, MSH6 and PMS2. Mutation carriers have an increased lifetime risk of developing colorectal cancer as well as other extracolonic tumours. The aim of...

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Detalhes bibliográficos
Main Authors: Loizidou, Maria A., Neophytou, Ioanna, Papamichael, Demetris, Kountourakis, Panteleimon, Vassiliou, Vassilios, Marcou, Yiola, Kakouri, Eleni, Ioannidis, Georgios, Philippou, Chrystalla, Spanou, Elena, Tanteles, George A., Anastasiadou, Violetta, Hadjisavvas, Andreas, Kyriacou, Kyriacos
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4136928/
https://ncbi.nlm.nih.gov/pubmed/25133505
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0105501
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