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Volumn 1, Issue 8, 1996, Pages 383-386
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Familial hypercholesterolemia and familial defective apolipoprotein B-100: comparison of the phenotypic expression In 116 cases.
a
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Author keywords
[No Author keywords available]
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Indexed keywords
APOLIPOPROTEIN B;
APOLIPOPROTEIN B100;
CHOLESTEROL;
LOW DENSITY LIPOPROTEIN RECEPTOR;
TRIACYLGLYCEROL;
ANGIOPLASTY;
ARTERIOSCLEROSIS;
ARTICLE;
BLOOD;
CAROTID ARTERY DISEASE;
COMPARATIVE STUDY;
CORONARY ARTERY BYPASS GRAFT;
CORONARY ARTERY DISEASE;
FEMALE;
GENETICS;
HEART INFARCTION;
HETEROZYGOTE DETECTION;
HOMOZYGOTE;
HUMAN;
HYPERCHOLESTEROLEMIA;
MALE;
PHENOTYPE;
POINT MUTATION;
RISK FACTOR;
STATISTICS;
ANGIOPLASTY;
APOLIPOPROTEIN B-100;
APOLIPOPROTEINS B;
ARTERIOSCLEROSIS;
CAROTID ARTERY DISEASES;
CHOLESTEROL;
CORONARY ARTERY BYPASS;
CORONARY DISEASE;
FEMALE;
HETEROZYGOTE DETECTION;
HOMOZYGOTE;
HUMANS;
HYPERCHOLESTEROLEMIA;
MALE;
MYOCARDIAL INFARCTION;
PHENOTYPE;
POINT MUTATION;
RECEPTORS, LDL;
RISK FACTORS;
TRIGLYCERIDES;
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EID: 0030599922
PISSN: 09492321
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (16)
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References (0)
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