Resequencing the APOE gene reveals that rare mutations are not significant contributory factors in the development of type III hyperlipidemia

Journal of Clinical Lipidology

Volumn 7, Issue 6, 2013, Pages 671-674

  Evans, David ^a   Beil, Frank Ulrich ^a   Aberle, Jens ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

Author keywords

APOE rare variants; Dyslipidemia; Hypertriglyceridemia; Resequencing; Type III hyperlipidemia

Indexed keywords

APOLIPOPROTEIN B; APOLIPOPROTEIN E; DNA; TRIACYLGLYCEROL;

ADULT; AGED; ARTICLE; CONTROLLED STUDY; DELETION MUTANT; DNA SEQUENCE; EXON; FEMALE; GENE MUTATION; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOTE; HUMAN; HYPERLIPIDEMIA; INTRON; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; PHENOTYPE; PRIORITY JOURNAL; TYPE III HYPERLIPIDEMIA;

APOE RARE VARIANTS; DYSLIPIDEMIA; HYPERTRIGLYCERIDEMIA; RESEQUENCING; TYPE III HYPERLIPIDEMIA;

ADULT; ALLELES; APOLIPOPROTEINS B; APOLIPOPROTEINS E; EXONS; FEMALE; GENOTYPE; HUMANS; HYPERLIPOPROTEINEMIA TYPE III; MALE; MIDDLE AGED; MUTATION; SEQUENCE ANALYSIS, DNA; TRIGLYCERIDES;

EID: 84889636421     PISSN: 19332874     EISSN: 18764789     Source Type: Journal    
DOI: 10.1016/j.jacl.2013.05.003     Document Type: Article

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