Two novel sequence variants in MSH2 gene in a patient who underwent cancer genetic counseling for a very early-onset epithelial ovarian cancer

BACKGROUND: Early-onset or hereditary ovarian cancer is mostly associated with BRCA1 or BRCA2 mutations. Mismatch repair genes sequence alteration frequently cause colorectal cancer, and, in less extent, other tumors, such as ovarian cancer. Subjects with personal and/or family history suggestive fo...

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Detalles Bibliográficos
Autores principales: Pensabene, Matilde, Condello, Caterina, Carlomagno, Chiara, De Placido, Sabino, Liccardo, Raffaella, Duraturo, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011803/
https://www.ncbi.nlm.nih.gov/pubmed/27602174
http://dx.doi.org/10.1186/s13053-016-0054-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011803/
https://www.ncbi.nlm.nih.gov/pubmed/27602174
http://dx.doi.org/10.1186/s13053-016-0054-5

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