Apolipoprotein E2/E2 genotype in combination with mutations in the LDL receptor gene causes type III hyperlipoproteinemia

Clinical Chemistry and Laboratory Medicine

Volumn 40, Issue 5, 2002, Pages 475-479

  Geisel, Jürgen ^a   Bunte, Thomas ^a   Bodis, Marion ^a   Oette, Kurt ^a   Herrmann, Wolfgang ^a  

^a SAARLAND UNIVERSITY   (Germany)

Author keywords

Atherosclerosis; Hypercholesterolemia; LDL receptor; SSCP analysis; Type III hyperlipidemia

Indexed keywords

APOLIPOPROTEIN E2; GLUTAMIC ACID; GLYCINE; ISOPROTEIN; LOW DENSITY LIPOPROTEIN CHOLESTEROL; LOW DENSITY LIPOPROTEIN RECEPTOR; TRIACYLGLYCEROL; VERY LOW DENSITY LIPOPROTEIN CHOLESTEROL; APOLIPOPROTEIN E; LIPID; LIPOPROTEIN;

ADULT; ALLELE; ARTICLE; CHOLESTEROL BLOOD LEVEL; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; EXON; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; GENOTYPE; HOMOZYGOSITY; HUMAN; HYPERLIPOPROTEINEMIA TYPE 3; LIPOPROTEIN BLOOD LEVEL; MALE; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN BLOOD LEVEL; SINGLE STRAND CONFORMATION POLYMORPHISM; TRIACYLGLYCEROL BLOOD LEVEL; BLOOD; GENETICS; HOMOZYGOTE; HYPOLIPOPROTEINEMIA; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE;

INSERTION SEQUENCES;

ADULT; APOLIPOPROTEIN E2; APOLIPOPROTEINS E; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HOMOZYGOTE; HUMANS; HYPOLIPOPROTEINEMIAS; LIPIDS; LIPOPROTEINS; MALE; MIDDLE AGED; MUTATION; RECEPTORS, LDL;

EID: 0036292960     PISSN: 14346621     EISSN: None     Source Type: Journal    
DOI: 10.1515/CCLM.2002.082     Document Type: Article

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