Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an example

Only approximately 50% of all familial breast cancers can be explained by known genetic factors, including mutations in BRCA1 and BRCA2. One of the most extensively studied candidates for breast and/or ovarian cancer susceptibility is BARD1. Although it was suggested that large mutations may contrib...

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Publicat a:Sci Rep
Autors principals: Klonowska, Katarzyna, Ratajska, Magdalena, Czubak, Karol, Kuzniacka, Alina, Brozek, Izabela, Koczkowska, Magdalena, Sniadecki, Marcin, Debniak, Jaroslaw, Wydra, Dariusz, Balut, Magdalena, Stukan, Maciej, Zmienko, Agnieszka, Nowakowska, Beata, Irminger-Finger, Irmgard, Limon, Janusz, Kozlowski, Piotr
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group 2015
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4439969/
https://ncbi.nlm.nih.gov/pubmed/25994375
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep10424
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