Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction

Keyphrases

• Recurrent Myocardial Infarction 100%
• Homozygous Familial Hypercholesterolemia (HoFH) 100%
• Family Members 20%
• Coronary Artery Disease 20%
• Exome Sequencing 13%
• Segregation Analysis 13%
• Myocardial Infarction Patients 13%
• Genetic Screening 6%
• Positive Family History 6%
• Autosomal Dominant 6%
• Clinical Phenotype 6%
• Myocardial Infarction 6%
• Family History 6%
• Cause of Disease 6%
• European Countries 6%
• Low-density Lipoprotein Receptor 6%
• Molecular Genetics 6%
• Disease Variants 6%
• Low-density Lipoprotein Cholesterol (LDL-C) 6%
• Proprotein Convertase Subtilisin Kexin Type 9 (PCSK9) 6%
• Oligogenic Disease 6%
• Premature Coronary Artery Disease 6%
• STAP1 6%
• Potential Diseases 6%
• Low-density Lipoprotein Cholesterol Level 6%
• Cholesterol-lowering 6%

Immunology and Microbiology

• Coronary Artery 100%
• Whole Exome Sequencing 50%
• Low Density Lipoprotein Cholesterol Level 25%
• Molecular Systematics 25%
• Genetic Screening 25%
• Autosomal Dominant Inheritance 25%
• Low-Density Lipoprotein 25%

Biochemistry, Genetics and Molecular Biology

• Familial Hypercholesterolemia 100%
• Exome Sequencing 13%
• Molecular Genetics 6%
• PCSK9 6%
• Autosomal Dominant Inheritance 6%
• Genetic Screening 6%
• Low Density Lipoprotein Cholesterol Level 6%
• Low-Density Lipoprotein 6%