A common genetic mechanism determines plasma apolipoprotein B levels and dense LDL subfraction distribution in familial combined hyperlipidemia

American Journal of Human Genetics

Volumn 63, Issue 2, 1998, Pages 586-594

  Juo, Suh Hang Hank ^a,b   Bredie, Sebastian J H ^c   Kiemeney, Lambertus A ^c   Demacker, Pierre N M ^c   Stalenhoef, Anton F H ^c,d  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b ROCKEFELLER UNIVERSITY   (United States)

^c RADBOUD UNIVERSITY NIJMEGEN   (Netherlands)

^d RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

APOLIPOPROTEIN B; CHOLESTEROL; LOW DENSITY LIPOPROTEIN; TRIACYLGLYCEROL;

ADULT; ARTICLE; CHOLESTEROL BLOOD LEVEL; FAMILIAL HYPERLIPEMIA; FEMALE; GENETIC ANALYSIS; HUMAN; HUMAN TISSUE; INHERITANCE; LIPID BLOOD LEVEL; MAJOR CLINICAL STUDY; MALE; MULTIFACTORIAL INHERITANCE; PARTICLE SIZE; PHENOTYPE; PLEIOTROPY; PRIORITY JOURNAL; SEGREGATION ANALYSIS; TRIACYLGLYCEROL BLOOD LEVEL;

EID: 0032231324     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/301962     Document Type: Article

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