INIS
mutations
100%
patients
100%
receptors
100%
density
100%
functional analysis
100%
lipoproteins
100%
apolipoproteins
100%
genetics
66%
cholesterol
33%
genes
33%
levels
33%
cardiovascular diseases
33%
screening
33%
proteins
33%
blood
33%
Keyphrases
Omani Patients
100%
Functional Analysis
100%
Homozygous Familial Hypercholesterolemia (HoFH)
100%
Apolipoprotein B (Apo B)
100%
Low-density Lipoprotein Receptor mutations
100%
Pathogenicity
25%
Genetic Variants
25%
Genetic Disorders
25%
Pathogenic mutations
25%
LDL Receptor
25%
Clinical Criteria
25%
Premature Cardiovascular Disease
25%
Functional Assay
25%
RIP1
25%
Low-density Lipoprotein Receptor
25%
Low-density Lipoprotein Cholesterol (LDL-C)
25%
Proprotein Convertase Subtilisin Kexin Type 9 (PCSK9)
25%
Medicine and Dentistry
Familial Hypercholesterolemia
100%
LDL Receptor
100%
Apolipoprotein B
100%
Genetic Disorder
25%
Proprotein Convertase 9
25%
Prematurity
25%
Genetic Variability
25%
Low Density Lipoprotein Cholesterol
25%
Cardiovascular Disease
25%
Receptor Protein
25%
Pathogenicity
25%