Frequency of ApoB and ApoE gene mutations as causes of hypobetalipoproteinemia in the Framingham offspring population

Arteriosclerosis, Thrombosis, and Vascular Biology

Volumn 18, Issue 11, 1998, Pages 1745-1751

  Welty, Francine K ^a,c   Lahoz, Carlos ^a   Tucker, Katherine L ^a   Ordovas, Jose M ^a   Wilson, Peter W F ^b   Schaefer, Ernst J ^a  

^a TUFTS UNIVERSITY   (United States)

^b FRAMINGHAM HEART STUDY   (United States)

^c BETH ISRAEL DEACONESS MEDICAL CENTER   (United States)

Author keywords

Apolipoproteins; Cancer; Coronary heart disease; Hypobetalipoproteinemia; LDL cholesterol

Indexed keywords

APOLIPOPROTEIN B; APOLIPOPROTEIN E; LOW DENSITY LIPOPROTEIN CHOLESTEROL;

ARTICLE; CANCER INCIDENCE; CHOLESTEROL BLOOD LEVEL; CROHN DISEASE; DISEASE ASSOCIATION; FAMILY HISTORY; GENE FREQUENCY; GENE MUTATION; GENETIC SUSCEPTIBILITY; HEMOCHROMATOSIS; HEPATITIS; HUMAN; HYPERLIPOPROTEINEMIA; MAJOR CLINICAL STUDY; PREVALENCE; PRIORITY JOURNAL; PROGENY; RISK ASSESSMENT;

EID: 0031771856     PISSN: 10795642     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.ATV.18.11.1745     Document Type: Article

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