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[phenomenon of strong association between the HLA B14 allele and the CYP21 V281L mutation found in this congenital adrenal hyperplasia population study can be used to distinguish between homozygote and hemizygote carrying the V281L mutation]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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Gene-disease associations inferred from text-mining the literature.
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