Genetic researches among Malaysian familial hypercholesterolaemic population

Genetic researches among Malaysian familial hypercholesterolaemic population

Background: Familial hypercholesterolaemia (FH) is one of the most frequent inherited metabolic disorders that can lead to a risk of premature cardiovascular disease. Publications on FH are mainly from western patients as there is little research on Asians, including Malaysians. The aim of this revi...

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Bibliographic Details
Main Authors: Al-Khateeb, A.R (Author), Al-Talib, H. (Author)
Format: Article
Language:English
Published: Faculty of Medicine, University of Malaya 2016
Subjects:
And proprotein convertase subtilisin kexin type 9
apolipoprotein B100
Apolipoprotein B-100
autosomal dominant inheritance
down regulation
endocytosis
exon
Familial hypercholesterolaemia
familial hypercholesterolemia
family history
genetic identification
genetic variability
genetics
genotype
genotype phenotype correlation
human
hyperlipidemia
loss of function mutation
low density lipoprotein cholesterol
low density lipoprotein receptor
Low-density lipoprotein receptor
Malaysian
Malaysians
molecular diagnosis
phenotype
prognosis
proprotein convertase 9
Review
single nucleotide polymorphism
xanthoma
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