ABCA1Alabama: A novel variant associated with HDL deficiency and premature coronary artery disease

Atherosclerosis

Volumn 164, Issue 2, 2002, Pages 245-250

  Seung, Ho Hong ^a   Rhyne, Jeffrey ^a   Zeller, Karen ^a   Miller, Michael ^a  

^a UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE   (United States)

Author keywords

ABCA1; Coronary artery disease; FHA; Low HDL cholesterol

Indexed keywords

ABC TRANSPORTER; GENOMIC DNA; HIGH DENSITY LIPOPROTEIN; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; LEUCINE; PROLINE;

ADULT; ALLELE; ARTICLE; CHILD; CHROMOSOME; CLINICAL ARTICLE; CONTROLLED STUDY; CORONARY ARTERY DISEASE; FAMILIAL DISEASE; FEMALE; GENE MUTATION; HETEROZYGOTE; HUMAN; HYPOALPHALIPOPROTEINEMIA; MALE; PRIORITY JOURNAL; PROTEIN FAMILY; SINGLE STRAND CONFORMATION POLYMORPHISM; TANGIER DISEASE;

ANGIOPLASTY, TRANSLUMINAL, PERCUTANEOUS CORONARY; ATP-BINDING CASSETTE TRANSPORTERS; BASE SEQUENCE; CHOLESTEROL, HDL; COMBINED MODALITY THERAPY; CORONARY ARTERIOSCLEROSIS; CORONARY ARTERY BYPASS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; POLYMERASE CHAIN REACTION; RISK ASSESSMENT; SENSITIVITY AND SPECIFICITY; SEQUENCE ANALYSIS, DNA; TANGIER DISEASE;

EID: 0036801569     PISSN: 00219150     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0021-9150(02)00106-5     Document Type: Article

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