High occurrence of BRCA1 intragenic rearrangements in hereditary breast and ovarian cancer syndrome in the Czech Republic

BACKGROUND: Alterations in the highly penetrant cancer susceptibility gene BRCA1 are responsible for the majority of hereditary breast and/or ovarian cancers. However, the number of detected germline mutations has been lower than expected based upon genetic linkage data. Undetected deleterious mutat...

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Detalhes bibliográficos
Main Authors: Vasickova, Petra, Machackova, Eva, Lukesova, Miroslava, Damborsky, Jiri, Horky, Ondrej, Pavlu, Hana, Kuklova, Jitka, Kosinova, Veronika, Navratilova, Marie, Foretova, Lenka
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2007
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1904436/
https://ncbi.nlm.nih.gov/pubmed/17561994
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-8-32
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