Familial Defective Apolipoprotein B-100 in a Group of Hypercholesterolaemic Patients in Poland. Identification of a New Mutation Thr3492Ile in the Apolipoprotein B Gene
European Journal of Human Genetics - United Kingdom
doi 10.1038/sj.ejhg.5200720
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November 1, 2001
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Springer Science and Business Media LLC