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Whole-exome sequencing of Finnish hereditary breast cancer families

A remarkable proportion of factors causing genetic predisposition to breast cancer (BC) are unknown in non-BRCA1/2 families. Exome sequencing was performed for 13 high-risk Finnish hereditary breast and/or ovarian cancer (HBOC) families to detect variants contributing to BC susceptibility. After fil...

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Detalhes bibliográficos
Publicado no:Eur J Hum Genet
Main Authors: Määttä, Kirsi, Rantapero, Tommi, Lindström, Anna, Nykter, Matti, Kankuri-Tammilehto, Minna, Laasanen, Satu-Leena, Schleutker, Johanna
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5159774/
https://ncbi.nlm.nih.gov/pubmed/27782108
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2016.141
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