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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/26641
Title: Homozygous DNA variants in exon 9 of the LDL receptor gene in a Thai patient with primary hypercholesterolemia phenotype
Authors: Klai Upsorn Pongrapeeporn
Preyanuj Yamwong
Wilairat Nuchpramool
Kosit Sribhen
Pikun Thepsuriyanon
Wattana Leowattana
Sompong Ong-Ajyooth
Mahidol University
Amersham Pharmacia Biotech.
Keywords: Medicine
Issue Date: 1-Dec-2001
Citation: Journal of the Medical Association of Thailand. Vol.84, No.SUPPL. 3 (2001)
Abstract: Mutation in low density lipoprotein (LDL) receptor gene causes an inherited primary hypercholesterolemia namely familial hypercholesterolemia (FH). In this study, 46 Thai patients with primary hypercholesterolemia were screened for mutations in exon 9 of the LDL receptor gene by polymerase chain reaction - restriction fragment length polymorphism (PCR - RFLP). The analysed fragment was 224 bp in length. According to the published cDNA sequence, exon 9 of the LDL receptor gene contains several hypermutable CpG dinucleotides. Three of these sites are Hpa II recognition sites. PCR product of exon 9 obtained from amplification of wild-type DNA sample would yield four fragments after Hpa II digestion. The expected sizes of these restriction fragments were 15, 30, 40 and 139 bp. All normocholesterolemic subjects (n = 33) showed normal RFLP. However, in one patient (72 year old female), abnormal RFLP from Hpa II digestion of the amplified exon 9 was observed, i.e., a fragment of 70 bp and another one smaller than 139 bp. Such RFLP reflects that exon 9 of both alleles of the LDL receptor gene in this patient lost one and gained one Hpa II site. It is interesting that this patient, eventhough harbouring two mutations on both alleles of the LDL receptor gene (presumably homozygous genotype of FH), apparently revealed lipid levels of heterozygous phenotype of FH without symptoms of coronary artery disease. It has yet to be proved whether these genetic variations are disease-related mutations or presumably common DNA polymorphisms.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0035749843&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/26641
ISSN: 01252208
Appears in Collections:Scopus 2001-2005

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