Autosomal recessive hypercholesterolemia

Seminars in Vascular Medicine

Volumn 4, Issue 3, 2004, Pages 241-248

  Soutar, Anne K ^a   Naoumova, Rossitza P ^a  

^a HAMMERSMITH HOSPITAL   (United Kingdom)

Author keywords

Aortic valve; Genetic disorder; LDL receptor pathway; Lipoprotein metabolism; Premature coronary disease; Xanthoma

Indexed keywords

ANTILIPEMIC AGENT; CLATHRIN; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE INHIBITOR; LOW DENSITY LIPOPROTEIN RECEPTOR; PHOSPHOLIPID; STATIN;

AUTOSOMAL RECESSIVE INHERITANCE; CELL FUNCTION; CELL MEMBRANE; CELL SURFACE; ENDOCYTOSIS; FAMILIAL HYPERCHOLESTEROLEMIA; GENE MUTATION; GENETIC DISORDER; HOMOZYGOSITY; HUMAN; ITALY; LIPOPROTEIN METABOLISM; LIVER; MIDDLE EAST; NONHUMAN; PHENOTYPE; PLASMA CLEARANCE; PROTEIN INTERACTION; REVIEW; XANTHOMA;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ANTILIPEMIC AGENTS; BLOOD COMPONENT REMOVAL; HUMANS; HYPERLIPOPROTEINEMIA TYPE II; MUTATION; PHENOTYPE; RECEPTORS, LDL;

EID: 11844273866     PISSN: 15289648     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-861491     Document Type: Review

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