BRCA1 and BRCA2 Mutations Other Than the Founder Alleles Among Ashkenazi Jewish in the Population of Argentina

In Ashkenazi Jewish (AJ) high risk families 3 mutations [2 in BRCA1 (c. 68_69del and c.5266dup) and 1 in BRCA2 (c.5946del)] account for the majority of high risk breast and ovarian cancer cases in that ethnic group. Few studies with limited number of genotyped individuals have expanded the spectrum...

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Autors principals:	Angela R. Solano, Natalia C. Liria, Fernanda S. Jalil, Daniela M. Faggionato, Pablo G. Mele, Alejandra Mampel, Florencia C. Cardoso, Ernesto J. Podesta
Format:	Artigo
Idioma:	Inglês
Publicat:	Frontiers Media S.A. 2018-08-01
Col·lecció:	Frontiers in Oncology
Matèries:	non-founder Ashkenazi BRCA1/2 mutations Ashkenazi Jewish hereditary breast and ovary cancer BRCA1 BRCA2
Accés en línia:	https://www.frontiersin.org/article/10.3389/fonc.2018.00323/full
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