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A founder mutation of the BRCA1 gene in Western Sweden associated with a high incidence of breast and ovarian cancer

✍ Scribed by Z Einbeigi; A Bergman; L.-G Kindblom; T Martinsson; J.M Meis-Kindblom; M Nordling; M Suurküla; J Wahlström; A Wallgren; P Karlsson

Book ID
117657327
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
115 KB
Volume
37
Category
Article
ISSN
0959-8049

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A high proportion of founder BRCA1 mutat
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## Abstract Three mutations in __BRCA1__ (5382insC, C61G and 4153delA) are common in Poland and account for the majority of mutations identified to date in Polish breast and breast–ovarian cancer families. It is not known, however, to what extent these 3 founder mutations account for all of the BRC

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Previous mutational analysis for BRCA gene mutations in sporadic ovarian cancer occurring in Chinese patients in Hong Kong identified six germline BRCA1 mutations and one germline BRCA2 mutation, six of which were novel (Khoo et al., 2000). Knowledge of BRCA gene mutations in the Chinese population