Human plasma CETP deficiency: Identification of a novel mutation in exon 9 of the CETP gene in a Caucasian subject from North America

Journal of Lipid Research

Volumn 39, Issue 2, 1998, Pages 442-456

  Teh, Evelyn M ^a   Dolphin, Peter J ^a   Breckenridge, W Carl ^a   Tan, Meng Hee ^a  

^a DALHOUSIE UNIVERSITY   (Canada)

Author keywords

Cholesteryl ester and phospholipid fatty acids; Cholesteryl ester transfer protein; HDL; Hyperalphalipoproteinemia; Mutation

Indexed keywords

CHOLESTEROL ESTER TRANSFER PROTEIN;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CHOLESTEROL TRANSPORT; CHROMOSOME 9; CORONARY RISK; DNA SEQUENCE; ESTERIFICATION; EXON; FEMALE; GENE MUTATION; HUMAN; HYPERCHOLESTEROLEMIA; LIPOPROTEIN DEFICIENCY; PRIORITY JOURNAL; VASCULAR ENDOTHELIUM;

APOLIPOPROTEIN A-I; APOLIPOPROTEINS B; APOLIPOPROTEINS E; CARRIER PROTEINS; CHOLESTEROL; CHOLESTEROL ESTER TRANSFER PROTEINS; EXONS; FEMALE; GLYCOPROTEINS; HOMOZYGOTE; HUMANS; HYPERCHOLESTEROLEMIA; HYPERTRIGLYCERIDEMIA; LIPOPROTEINS, HDL; LIPOPROTEINS, LDL; LIPOPROTEINS, VLDL; MIDDLE AGED; MUTATION; NOVA SCOTIA; PHOSPHATIDYLCHOLINE-STEROL O-ACYLTRANSFERASE;

EID: 0031910644     PISSN: 00222275     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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