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Volumn 33, Issue 2, 2001, Pages 122-126
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Apolipoprotein B Arg3500Gln mutation prevalence in children with hypercholesterolemia: A french multicenter study
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Author keywords
Apolipoprotein B; Familial combined hyperlipidemia; Familial defective apo B 100; Hypercholesterolemia; Polygenic hypercholesterolemia
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Indexed keywords
APOLIPOPROTEIN B;
ARGININE;
LOW DENSITY LIPOPROTEIN CHOLESTEROL;
ADOLESCENT;
ARTICLE;
CARDIOVASCULAR DISEASE;
CARDIOVASCULAR RISK;
CHILD;
CHOLESTEROL BLOOD LEVEL;
CONTROLLED STUDY;
FAMILIAL HYPERCHOLESTEROLEMIA;
FEMALE;
GENE MUTATION;
GENETIC SCREENING;
HUMAN;
HYPERLIPIDEMIA;
INFANT;
MALE;
MASS SCREENING;
PHENOTYPE;
POLYMERASE CHAIN REACTION;
PREVALENCE;
PRIORITY JOURNAL;
RESTRICTION MAPPING;
ADOLESCENT;
APOLIPOPROTEIN B-100;
APOLIPOPROTEINS B;
CARDIOVASCULAR DISEASES;
CHILD;
CHILD, PRESCHOOL;
CHOLESTEROL, LDL;
FEMALE;
FRANCE;
GENE FREQUENCY;
HUMANS;
HYPERLIPOPROTEINEMIA TYPE II;
INFANT;
MALE;
MUTATION;
PHENOTYPE;
POLYMERASE CHAIN REACTION;
PREVALENCE;
RESTRICTION MAPPING;
RISK FACTORS;
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EID: 17944378174
PISSN: 02772116
EISSN: None
Source Type: Journal
DOI: 10.1097/00005176-200108000-00005 Document Type: Article |
Times cited : (14)
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References (38)
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