Association of FANCM Mutations with Familial and Early-Onset Breast Cancer Risk in a South American Population

Breast cancer (BC) is the most common cancer among women worldwide. BRCA1/2 are responsible for 16–20% of the risk for hereditary BC. Other susceptibility genes have been identified; Fanconi Anemia Complementation Group M (FANCM) being one of these. Two variants in FANCM, rs144567652 and rs147021911...

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Detalles Bibliográficos
Autores principales: Morales-Pison, Sebastian, Morales-González, Sarai, Fernandez-Ramires, Ricardo, Tapia, Julio C., Maldonado, Edio, Calaf, Gloria M., Jara, Lilian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9959766/
https://www.ncbi.nlm.nih.gov/pubmed/36835452
http://dx.doi.org/10.3390/ijms24044041

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9959766/
https://www.ncbi.nlm.nih.gov/pubmed/36835452
http://dx.doi.org/10.3390/ijms24044041

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