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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Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Front Oncol
Päätekijät: Solano, Angela R., Liria, Natalia C., Jalil, Fernanda S., Faggionato, Daniela M., Mele, Pablo G., Mampel, Alejandra, Cardoso, Florencia C., Podesta, Ernesto J.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Frontiers Media S.A. 2018
Aiheet:
Oncology
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6113569/
https://ncbi.nlm.nih.gov/pubmed/30186769
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fonc.2018.00323
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