Breast Cancer

Multi-exonic BRCA1 deletion identified through single nucleotide polymorphism

Published in Cancer Gene Therapy Week, May 16th, 2005

Researchers were able to identify a multi-exonic BRCA1 deletion through a single nucleotide polymorphism.

According to published research from the United States, "The identification of intragenic rearrangements is important for a comprehensive understanding of mutations that occur in some clinically important genes. Single nucleotide polymorphism haplotypes obtained from clinical sequence data have been used to identify patients at high risk for rearrangement mutations. Application of this method identified a novel 26-kb deletion of BRCA1 exons 14 through 20 in patients from multiple families with hereditary breast and ovarian cancer."

"Clinical...

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Source: Cancer Gene Therapy Week (2005-05-16)

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