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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4136928/
https://www.ncbi.nlm.nih.gov/pubmed/25133505
http://dx.doi.org/10.1371/journal.pone.0105501

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