Pages that link to "Q33676491"

The following pages link to Haplotype associations of three DNA polymorphisms at the human low density lipoprotein receptor gene locus in familial hypercholesterolaemia (Q33676491):

Displaying 12 items.

• The use of low density lipoprotein receptor activity of lymphocytes to determine the prevalence of familial hypercholesterolaemia in a rural South African community (Q33592707) (← links)
• An exon 4 mutation identified in the majority of South African familial hypercholesterolaemics (Q33597678) (← links)
• Medical genetics in South Africa (Q33598374) (← links)
• Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus (Q33598443) (← links)
• Familial hypercholesterolaemia in South Africans: tracking findings and developments over time - with reference to : prevalence of hypercholesterolaemia in young Afrikaners with myocardial infarction. Ischaemic heart disease risk factors (Q34365982) (← links)
• Predominance of a 6 bp deletion in exon 2 of the LDL receptor gene in Africans with familial hypercholesterolaemia. (Q35435218) (← links)
• Molecular genetic evidence for a founder effect in familial hypercholesterolemia among French Canadians (Q41089337) (← links)
• Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry (Q45041602) (← links)
• CpG hotspot mutations at the LDL receptor locus are a frequent cause of familial hypercholesterolemia among South African Indians (Q46426785) (← links)
• A de novo duplication in the low density lipoprotein receptor gene (Q46527972) (← 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)
• A new LDL receptor gene deletion mutation in the South African population (Q67980053) (← links)