Haplotype analysis of the 185delAG BRCA1 mutation in ethnically diverse populations

The 185delAG* BRCA1 mutation is encountered primarily in Jewish Ashkenazi and Iraqi individuals, and sporadically in non-Jews. Previous studies estimated that this is a founder mutation in Jewish mutation carriers that arose before the dispersion of Jews in the Diaspora ∼2500 years ago. The aim of t...

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Bibliografiset tiedot
Päätekijät: Laitman, Yael, Feng, Bing-Jian, Zamir, Itay M, Weitzel, Jeffrey N, Duncan, Paul, Port, Danielle, Thirthagiri, Eswary, Teo, Soo-Hwang, Evans, Gareth, Latif, Ayse, Newman, William G, Gershoni-Baruch, Ruth, Zidan, Jamal, Shimon-Paluch, Shani, Goldgar, David, Friedman, Eitan
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group 2013
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3548269/
https://ncbi.nlm.nih.gov/pubmed/22763381
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2012.124
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