Identification and characterization of novel low-density lipoprotein receptor mutations of familial hypercholesterolaemia patients in Taiwan

Medicine and Dentistry

• Familial Hypercholesterolemia 100%
• LDL Receptor 100%
• Receptor Gene 42%
• Receptor 28%
• Missense Mutation 28%
• Exon 28%
• In Vitro 14%
• Disease 14%
• Point Mutation 14%
• DNA Sequence 14%
• Allele 14%
• Vascular Disease 14%
• Gene Mutation 14%
• Apolipoprotein 14%
• Autosomal Dominant Inheritance 14%
• Nonsense Mutation 14%
• Pedigree 14%
• Multiplex Polymerase Chain Reaction 14%

Biochemistry, Genetics and Molecular Biology

• LDL Receptor 100%
• Familial Hypercholesterolemia 100%
• Receptor Gene 42%
• Exon 28%
• Missense Mutation 28%
• Missense 28%
• Eicosanoid Receptor 28%
• Point Mutation 14%
• Multiplex Polymerase Chain Reaction 14%
• Allele 14%
• DNA Sequence 14%
• Apolipoprotein 14%
• Gene Mutation 14%
• Pedigree 14%
• Nonsense Mutation 14%
• Autosomal Dominant Inheritance 14%