BRCA1 founder mutations and beyond in the Polish population: A single-institution BRCA1/2 next-generation sequencing study

Hereditary mutations in BRCA1/2 genes increase the risk of breast cancer by 60–80% and ovarian cancer by about 20–40% in female carriers. Detection of inherited mutations in asymptomatic carriers allows for the implementation of appropriate preventive measures. BRCA1/2 genotyping is also important f...

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發表在:PLoS One
Main Authors: Kowalik, Artur, Siołek, Monika, Kopczyński, Janusz, Krawiec, Kamila, Kalisz, Joanna, Zięba, Sebastian, Kozak-Klonowska, Beata, Wypiórkiewicz, Elżbieta, Furmańczyk, Jowita, Nowak-Ozimek, Ewelina, Chłopek, Małgorzata, Macek, Paweł, Smok-Kalwat, Jolanta, Góźdź, Stanisław
格式: Artigo
語言:Inglês
出版: Public Library of Science 2018
主題:
Research Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6057642/
https://ncbi.nlm.nih.gov/pubmed/30040829
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0201086
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