No abstract available
MeSH terms
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Apolipoproteins E / genetics*
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Cholesterol / blood
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Chromosome Mapping
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Chromosomes, Human, 19-20
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Genotype
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Homozygote
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Humans
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Hyperlipoproteinemia Type II / genetics
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Hyperlipoproteinemias / genetics*
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Mutation
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Myocardial Infarction / genetics*
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Phenotype
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Polymorphism, Genetic*
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Risk
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Triglycerides / blood
Substances
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Apolipoproteins E
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Triglycerides
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Cholesterol