Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families
Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families
About this item
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Author / Creator
Osher, D J , De Leeneer, K , Michils, G , Hamel, N , Tomiak, E , Poppe, B , Leunen, K , Legius, E , Shuen, A , Smith, E , Arseneau, J , Tonin, P , Matthijs, G , Claes, K , Tischkowitz, M D and Foulkes, W D
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
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Publication information
Publisher
London: Nature Publishing Group UK
Subjects
More information
Scope and Contents
Contents
Background:
Recent data show that mutations in
RAD51D
have an aetiological role in ovarian carcinoma, yet mutations do not appear to be associated with an increased risk for breast cancer. We studied ovarian and breast cancer families having at least one woman affected by ovarian carcinoma, to assess the importance of
RAD51D
mutation...
Alternative Titles
Full title
Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families
Authors, Artists and Contributors
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Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3326673
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3326673
Other Identifiers
ISSN
0007-0920
E-ISSN
1532-1827
DOI
10.1038/bjc.2012.87
