A novel nonsense apolipoprotein A-I mutation (apoA-IE136X) causes low HDL cholesterol in French Canadians

Atherosclerosis

Volumn 185, Issue 1, 2006, Pages 127-136

  Dastani, Zari ^a   Dangoisse, Carole ^a   Boucher, Betsie ^a   Desbiens, Katia ^a   Krimbou, Larbi ^a   Dufour, Robert ^b   Hegele, Robert A ^c   Pajukanta, Päivi ^d   Engert, James C ^a   Genest, Jacques ^a   Marcil, Michel ^a  

^a ROYAL VICTORIA HOSPITAL   (Canada)

^b CLIN RESEARCH INSTITUTE OF MONTREAL   (Canada)

^c ROBARTS RESEARCH INSTITUTE   (Canada)

^d UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Apolipoprotein A I; Coronary artery disease; French Canadian population; Gene mutation; High density lipoprotein deficiency; Hypoalphalipoproteinemia

Indexed keywords

APOLIPOPROTEIN A1; HIGH DENSITY LIPOPROTEIN; MUTANT PROTEIN; PHOSPHATIDYLCHOLINE STEROL ACYLTRANSFERASE;

ADULT; ARTICLE; CONTROLLED STUDY; CORONARY ARTERY DISEASE; DISEASE ASSOCIATION; DISEASE COURSE; DNA SEQUENCE; ETHNIC GROUP; FEMALE; GENETIC ANALYSIS; HUMAN; LIPOPROTEIN BLOOD LEVEL; LIPOPROTEIN DEFICIENCY; MALE; NONSENSE MUTATION; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN SECRETION;

ADOLESCENT; ADULT; AGED; APOLIPOPROTEIN A-I; CANADA; CHILD; CHOLESTEROL, HDL; CODON, NONSENSE; CORONARY DISEASE; DNA; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; FEMALE; FRANCE; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; MALE; MIDDLE AGED; PEDIGREE; POLYMERASE CHAIN REACTION; TANGIER DISEASE;

EID: 30944435268     PISSN: 00219150     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.atherosclerosis.2005.05.028     Document Type: Article

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