Hereditary predisposition to breast cancer:evaluating the role of rare copy number variant, protein-truncating and missense candidate alleles

Abstract Breast cancer is the most common cancer among women, and inherited predisposition is one of the major recognized causes of increased breast cancer risk. Only about half of the hereditary cases are explained by mutations in the known susceptibility genes, including the DNA damage response g...

Full description

Bibliographic Details
Main Author: Tervasmäki, A. (Anna)
Other Authors: Pylkäs, K. (Katri)
Format: Doctoral Thesis
Language:English
Published: Oulun yliopisto 2018
Subjects:
Online Access:http://urn.fi/urn:isbn:9789526220826
http://nbn-resolving.de/urn:isbn:9789526220826