Characterization of a novel cellular defect in patients with phenotypic homozygous familial hypercholesterolemia
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Reference34 articles.
1. Influence of genotype at the low density lipoprotein (LDL) receptor gene locus on the clinical phenotype and response to lipid-lowering drug therapy in heterozygous familial hypercholesterolaemia
2. Comparison of the Genetic Defect with LDL-Receptor Activity in Cultured Cells from Patients With a Clinical Diagnosis of Heterozygous Familial Hypercholesterolemia
3. Phenotypic Variation in Heterozygous Familial Hypercholesterolemia
4. Spectrum of LDL receptor gene mutations in heterozygous familial hypercholesterolemia
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