Abstract
A DNA sequence polymorphism, revealed by digestion of human DNA with the restriction endonuclease Sst-1 and hybridization with an apolipoprotein A-I complementary DNA clone, has been shown to be located in or close to the 3' noncoding region of the apolipoprotein C-III gene. This polymorphism is found in significantly increased prevalence (P less than 0.001) in Caucasian hypertriglyceridemic subjects compared with race-matched controls, and its distribution in normal individuals of differing racial origins is reported. Furthermore, no alteration of high density lipoprotein or apolipoprotein A-I and apolipoprotein C-III phenotypes was observed in individuals with or without the polymorphism.
MeSH Terms
Adolescent
Apolipoprotein A-I
Apolipoprotein C-III
Apolipoproteins A/blood,genetics
Apolipoproteins C/blood,genetics
Child
China/ethnology
DNA/genetics
DNA Restriction Enzymes/metabolism
Deoxyribonucleases, Type II Site-Specific
Female
Genes
Genotype
Humans
Hyperlipoproteinemia Type IV/genetics
Isoelectric Focusing
Lipoproteins, HDL/blood
Male
Pedigree
Polymorphism, Genetic
Whites
Chemicals
Apolipoprotein A-I
Apolipoprotein C-III
Apolipoproteins A
Apolipoproteins C
Lipoproteins, HDL
DNA
DNA Restriction Enzymes
endodeoxyribonuclease SacI
Deoxyribonucleases, Type II Site-Specific
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Rees A
Stocks J
Sharpe C R
Vella M A
Shoulders C C
Katz J
Jowett N I
Baralle F E
Galton D J
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