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[A cohort of 236 apparently unrelated patients with clinical features of FH was screened for a common mutation causing familial defective apolipoprotein B-100 (FDB) and seven low-density lipoprotein receptor (LDLR) gene defects known to be relatively common in South Africans with FH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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