Genetic variants of ApoE account for variability of plasma low-density lipoprotein and apolipoprotein B levels in FHBL

Atherosclerosis

Volumn 178, Issue 1, 2005, Pages 107-113

  Yue, Pin ^a   Isley, William L ^b   Harris, William S ^b   Rosipal, Stefan ^c   Akin, Carl D ^d   Schonfeld, Gustav ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

^b UNIVERSITY OF MISSOURI KANSAS CITY   (United States)

^c Department of Pediatrics   (Slovakia)

^d 1515 W Truman Rd   (United States)

Author keywords

ApoB; ApoB truncation; Apolipoprotein E; FHBL; LDL cholesterol

Indexed keywords

APOLIPOPROTEIN B; APOLIPOPROTEIN E; GLUTAMIC ACID; LOW DENSITY LIPOPROTEIN; LOW DENSITY LIPOPROTEIN CHOLESTEROL; TYROSINE;

ADULT; ARTICLE; CODON; CONTROLLED STUDY; EXON; FRAMESHIFT MUTATION; GENE DELETION; GENE MUTATION; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOSITY; HUMAN; HUMAN CELL; HYPOBETALIPOPROTEINEMIA; MULTIGENE FAMILY; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

ADULT; APOLIPOPROTEINS B; APOLIPOPROTEINS E; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENOTYPE; GLUTAMIC ACID; GUANINE; HUMANS; HYPOBETALIPOPROTEINEMIAS; LIPOPROTEINS, LDL; MALE; PEDIGREE; PHENOTYPE; POINT MUTATION; THYMINE; TYROSINE; VARIATION (GENETICS);

EID: 10044237830     PISSN: 00219150     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.atherosclerosis.2004.06.020     Document Type: Article

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