Pages that link to "Q33678390"

The following pages link to Identification of a common low density lipoprotein receptor mutation (R329X) in the south of England: complete linkage disequilibrium with an allele of microsatellite D19S394. (Q33678390):

Displaying 15 items.

• The type of mutation in the low density lipoprotein receptor gene influences the cholesterol-lowering response of the HMG-CoA reductase inhibitor simvastatin in patients with heterozygous familial hypercholesterolaemia (Q28373582) (← links)
• Rapid sizing of microsatellite alleles by gel electrophoresis on microfabricated channels: application to the D19S394 tetranucleotide repeat for cosegregation study of familial hypercholesterolemia (Q31029019) (← links)
• Identification of a common low density lipoprotein receptor mutation (C163Y) in the west of Scotland (Q33680998) (← links)
• Characterization of a novel cellular defect in patients with phenotypic homozygous familial hypercholesterolemia (Q33857941) (← links)
• Candidate-Gene Studies of the Atherogenic Lipoprotein Phenotype: A Sib-Pair Linkage Analysis of DZ Women Twins (Q34384470) (← links)
• LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis (Q34650934) (← links)
• LDL-receptor mutations in Europe (Q35938094) (← links)
• Analysis of the frequency and spectrum of mutations recognised to cause familial hypercholesterolaemia in routine clinical practice in a UK specialist hospital lipid clinic (Q36983486) (← links)
• A "de novo" mutation of the LDL-receptor gene as the cause of familial hypercholesterolemia (Q43992160) (← links)
• Allelic variation in the promoter region of the LDL receptor gene: analysis of an African-specific variant in the FP2 cis-acting regulatory element (Q46529734) (← links)
• Update of the molecular basis of familial hypercholesterolemia in The Netherlands (Q46775373) (← links)
• Mutational analysis in UK patients with a clinical diagnosis of familial hypercholesterolaemia: relationship with plasma lipid traits, heart disease risk and utility in relative tracing (Q46876618) (← links)
• Fine mapping of low-density lipoprotein receptor gene by genetic linkage on chromosome 19p13.1-p13.3 and study of the founder effect of four French Canadian low-density lipoprotein receptor gene mutations (Q57316332) (← links)
• Identification and characterization of LDL receptor gene mutations in hyperlipidemic Chinese (Q73600046) (← links)
• Heritability Analysis of Lipids and Three Gene Loci in Twins Link the Macrophage Scavenger Receptor to HDL Cholesterol Concentrations (Q73832923) (← links)