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