Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten cases

Keyphrases

• Clinical Characteristics 100%
• Scandinavia 100%
• Apolipoprotein B-100 100%
• Homozygous Familial Hypercholesterolemia (HoFH) 100%
• United Kingdom 100%
• Clinical Diagnosis 66%
• Unrelated Individuals 66%
• Denmark 33%
• Low-density Lipoprotein Cholesterol (LDL-C) 33%
• Moderate to Severe 33%
• Exon 33%
• Screening Method 33%
• Serum Concentration 33%
• Molecular Screening 33%
• As(III) 33%
• Subclinical Cardiovascular Disease 33%
• Codon 33%
• Amino Acids 33%
• Plasma Lipid Levels 33%
• Arginine 33%
• Glutamine 33%
• Apolipoprotein B Gene 33%
• Genetic Disease 33%
• Low-density Lipoprotein Receptor 33%
• Severe Hypercholesterolemia 33%
• Level Characteristic Values 33%

Biochemistry, Genetics and Molecular Biology

• Apolipoprotein B 100%
• Familial Hypercholesterolemia 75%
• Hyperlipidemia 75%
• Blood Level 25%
• Exon 25%
• Amino Acids 25%
• LDL Receptor 25%
• Blood Lipids 25%
• Codon 25%
• Lipid Level 25%
• Genetic Disorder 25%
• Hypercholesterolemia 25%
• Glutamine 25%
• Low-Density Lipoprotein 25%
• Arginine 25%
• Cholesterol 25%