Molecular basis of familial hypercholesterolemia

Research output: Contribution to journalReview article

45 Scopus citations

Abstract

Familial hypercholesterolemia (FH) is a genetic disease characterized by an elevated level of low density lipoprotein (LDL), xanthomas, and an increased frequency of heart attacks. One of the first descriptions of this disease was reported some 50 years ago by the Norwegian physician, Carl Muller. Research and clinical studies in the ensuing half century have shown that FH is caused by mutations in the gene for the LDL receptor. In this article, we review our studies of the last 5 years that have focused on the molecular genetics of the LDL receptor locus and its pathogenesis in FH.

Original languageEnglish (US)
Pages (from-to)I8-I13
JournalArteriosclerosis
Volume9
Issue number1 SUPPL.
StatePublished - Jan 1 1989

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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