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[No sequence alterations were found in 80 nonfamilial ESCC cases (P=0.01) and 100 healthy controls (P=0.0037), suggesting that germ line BRCA2 gene mutation may play a role in familial aggregation of ESCC in high-risk region of India.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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