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dc.contributor.authorKlai Upsorn S. Pongrapeepornen_US
dc.contributor.authorVallaya Sutthikhumen_US
dc.contributor.authorAtip Likidliliden_US
dc.contributor.authorSaiphon Poldeeen_US
dc.contributor.authorAree Futrakulen_US
dc.contributor.authorPreyanuj Yamwongen_US
dc.contributor.authorAnchalee Amornrattanaen_US
dc.contributor.authorSompong Ong-Ajyoothen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-07T09:16:41Z-
dc.date.available2018-09-07T09:16:41Z-
dc.date.issued2000-11-01en_US
dc.identifier.citationJournal of the Medical Association of Thailand. Vol.83, No.SUPPL. 2 (2000)en_US
dc.identifier.issn01252208en_US
dc.identifier.other2-s2.0-0034328420en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0034328420&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/26122-
dc.description.abstractA mutation in low density lipoprotein (LDL) receptor gene causes an autosomal codominant disorder namely familial hypercholesterolemia (FH). Mutations in the LDL receptor gene are very heterogeneous at the DNA levels, occurring in all 18 exons of the gene. However, exon 4 has been found to be the hot spot for mutational events. In this study DNA from 45 Thai subjects with primary hypercholesterolemia was screened for mutations in the hot spot exon 4. The DNA samples were amplified by Polymerase Chain Reaction (PCR) and screened for mutation by Cleavase Fragment Length Polymorphism (CFLP) technique. Identification of mutation was per-formed by direct sequencing of PCR product. From this screening, one female patient was found to be heterozygous for a novel mutation which was due to a G to T transversion at nucleotide 514. This transversion would change the species-conserved amino acid at codon 151 from charged R group aspatic (GAC) to uncharged R group tyrosine (TAC), termed D151Y. From the same screening strategy, we found that this mutation was absent in 33 healthy normolipidemic subjects. In this index subject, Arg 3500 Gln mutation in apo B-100 gene, causing hypercholesterolemia namely familial defective apo B-100 (FDB), was not found. Therefore, hypercholesterolemia in this index subject was possibly caused by the D151Y mutation in the LDL receptor gene.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0034328420&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleScreening for mutations in exon 4 of the LDL receptor gene in Thai subjects with primary hypercholesterolemia: Detection of a novel mutation D151Y by PCR-CFLPen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
Appears in Collections:Scopus 1991-2000

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