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Volumn 33, Issue 2, 2001, Pages 119-121
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Monogenic disorders that cause LDL cholesterol to accumulate in plasma
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Author keywords
[No Author keywords available]
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Indexed keywords
ABC TRANSPORTER;
APOLIPOPROTEIN B;
CHOLESTEROL;
GENE PRODUCT;
HIGH DENSITY LIPOPROTEIN CHOLESTEROL;
LOW DENSITY LIPOPROTEIN CHOLESTEROL;
LOW DENSITY LIPOPROTEIN RECEPTOR;
TRIACYLGLYCEROL;
AUTOSOMAL RECESSIVE DISORDER;
CELL TRANSPORT;
CHOLESTEROL BLOOD LEVEL;
CHOLESTEROL INTAKE;
CHOLESTEROL METABOLISM;
CHOLESTEROL SYNTHESIS;
CHOLESTEROL TRANSPORT;
DIET;
EDITORIAL;
FAMILIAL HYPERCHOLESTEROLEMIA;
GENE MUTATION;
HUMAN;
HYPERCHOLESTEROLEMIA;
LIVER METABOLISM;
MONOGENIC DISORDER;
PRIORITY JOURNAL;
APOLIPOPROTEIN B-100;
APOLIPOPROTEINS B;
CHILD;
CHOLESTEROL;
CHOLESTEROL, LDL;
GENETIC PREDISPOSITION TO DISEASE;
HUMANS;
HYPERLIPOPROTEINEMIA TYPE II;
MUTATION;
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EID: 0034860472
PISSN: 02772116
EISSN: None
Source Type: Journal
DOI: 10.1097/00005176-200108000-00004 Document Type: Editorial |
Times cited : (1)
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References (6)
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