Spectrum of BRCA1/2 variants in 940 patients from Argentina including novel, deleterious and recurrent germline mutations: impact on healthcare and clinical practice

BRCA1/2 mutations in Latin America are scarcely documented and in serious need of knowledge about the spectrum of BRCA pathogenic variants, information which may alter clinical practice and subsequently improve patient outcome. In addition, the search for data on testing policies in different region...

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Detalles Bibliográficos
Autores principales: Solano, Angela Rosaria, Cardoso, Florencia Cecilia, Romano, Vanesa, Perazzo, Florencia, Bas, Carlos, Recondo, Gonzalo, Santillan, Francisco Bernardo, Gonzalez, Eduardo, Abalo, Eduardo, Viniegra, María, Michel, José Davalos, Nuñez, Lina María, Noblia, Cristina Maria, Mc Lean, Ignacio, Canton, Enrique Diaz, Chacon, Reinaldo Daniel, Cortese, Gustavo, Varela, Eduardo Beccar, Greco, Martín, Barrientos, María Laura, Avila, Silvia Adela, Vuotto, Hector Daniel, Lorusso, Antonio, Podesta, Ernesto Jorge, Mando, Oscar Gaspar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Clinical Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601155/
https://www.ncbi.nlm.nih.gov/pubmed/28947987
http://dx.doi.org/10.18632/oncotarget.10814

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601155/
https://www.ncbi.nlm.nih.gov/pubmed/28947987
http://dx.doi.org/10.18632/oncotarget.10814

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