Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population

Journal of Clinical Investigation

Volumn 114, Issue 9, 2004, Pages 1343-1353

  Frikke Schmidt, Ruth ^a   Nordestgaard, Børge G ^b,c   Jensen, Gorm B ^c   Tybjærg Hansen, Anne ^a,c  

^a University of Copenhagen   (Denmark)

^b GENTOFTE UNIVERSITY HOSPITAL   (Denmark)

^c BISPEBJERG HOSPITAL   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER A1; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; ABC TRANSPORTER;

ABCA1 GENE; ADULT; ARTICLE; FEMALE; GENE; GENE MUTATION; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; MALE; NUCLEOTIDE SEQUENCE; POPULATION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; TANGIER DISEASE; 5' UNTRANSLATED REGION; AGED; ALLELE; AMINO ACID SEQUENCE; ANIMAL; BIOLOGICAL MODEL; BLOOD; GENETICS; HAPLOTYPE; HETEROZYGOTE; HOMOZYGOTE; MIDDLE AGED; MOLECULAR GENETICS; MOUSE; MUTATION; PROMOTER REGION; PROTEIN TERTIARY STRUCTURE; SEQUENCE HOMOLOGY;

5' UNTRANSLATED REGIONS; ADULT; AGED; AGED, 80 AND OVER; ALLELES; AMINO ACID SEQUENCE; ANIMALS; ATP-BINDING CASSETTE TRANSPORTERS; CHOLESTEROL, HDL; FEMALE; GENOTYPE; HAPLOTYPES; HETEROZYGOTE; HOMOZYGOTE; HUMANS; MALE; MICE; MIDDLE AGED; MODELS, BIOLOGICAL; MOLECULAR SEQUENCE DATA; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; PROMOTER REGIONS (GENETICS); PROTEIN STRUCTURE, TERTIARY; SEQUENCE HOMOLOGY, AMINO ACID; VARIATION (GENETICS);

EID: 14644420598     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI200420361     Document Type: Article

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