Double Heterozygotes for the Ashkenazi Founder Mutations in BRCA1 and BRCA2 Genes

This publication has 8 references indexed in Scilit:

• The 185delAG BRCA1 mutation originated before the dispersion of Jews in the diaspora and is not limited to Ashkenazim
  Human Molecular Genetics, 1998
• Co-segregation of BRCA1 185delAG mutation and BRCA2 6174delT in one single family
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• The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%
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• Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2
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• The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals
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• A human BRCA1 gene knockout
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