Absence of ABCA1 mutations in individuals with low serum HDL-cholesterol [1]

Clinical Chemistry

Volumn 49, Issue 3, 2003, Pages 521-522

  Woll, Petter S ^a   Hanson, Naomi Q ^a   Tsai, Michael Y ^a,b  

^a UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^b Mayo Mail Code 609   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

APOLIPOPROTEIN C2; APOLIPOPROTEIN C3; CHOLESTEROL; CHOLESTEROL ESTER TRANSFER PROTEIN; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; LIPOPROTEIN LIPASE; TRIACYLGLYCEROL; TRIACYLGLYCEROL LIPASE;

ABCA1 GENE; ADULT; AGED; ALLELE; ATHEROSCLEROSIS; CAUCASIAN; CHOLESTEROL BLOOD LEVEL; CHROMOSOME 9Q; CONTROLLED STUDY; CORONARY ARTERY BYPASS GRAFT; ETHNIC DIFFERENCE; ETHNIC GROUP; FEMALE; GENE; GENE FREQUENCY; GENE IDENTIFICATION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC CODE; GENETIC LINKAGE; GENETIC POLYMORPHISM; GENETIC SCREENING; GENETIC VARIABILITY; HETEROZYGOTE; HUMAN; HYPOLIPOPROTEINEMIA; ISCHEMIC HEART DISEASE; LETTER; LIPID METABOLISM; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; PREVALENCE; REGULATORY MECHANISM; TANGIER DISEASE; TURNOVER TIME;

ADOLESCENT; ADULT; AGED; ATP-BINDING CASSETTE TRANSPORTERS; CARDIOVASCULAR DISEASES; CHOLESTEROL, HDL; CORONARY ARTERIOSCLEROSIS; CORONARY ARTERY BYPASS; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION; MYOCARDIAL INFARCTION;

EID: 0037370089     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1373/49.3.521     Document Type: Letter

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