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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/18325
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dc.contributor.authorH. Furuumien_US
dc.contributor.authorN. Firdousen_US
dc.contributor.authorT. Inoueen_US
dc.contributor.authorH. Ohtaen_US
dc.contributor.authorP. Winichagoonen_US
dc.contributor.authorS. Fucharoenen_US
dc.contributor.authorY. Fukumakien_US
dc.contributor.otherKyushu Universityen_US
dc.contributor.otherSociety for Health Educationen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-04T08:04:27Z-
dc.date.available2018-07-04T08:04:27Z-
dc.date.issued1998-01-01en_US
dc.identifier.citationHemoglobin. Vol.22, No.2 (1998), 141-151en_US
dc.identifier.issn03630269en_US
dc.identifier.other2-s2.0-0031897372en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0031897372&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/18325-
dc.description.abstractWe have systematically analyzed β-thalassemia genes using polymerase chain reaction-related techniques, dot-blot hybridization with oligonucleotide probes, allele specific-polymerase chain reaction, and sequencing of amplified DNA fragments from 41 unrelated patients, including 37 β-thalassemia homozygotes, three with β-thalassemia/Hb E, and one with β-thalassemia/Hb S. Four different β-thalassemia mutations were detected in 78 alleles. These are the IVS-I-5 (G→C), codon 30 (AGG→ACG) [also indicated as IVS-I (-1)], IVS-I-1 (G→A), and codons 41/42 (-TTCT) mutations. The distribution of the β-thalassemia mutations in the Maldives is 58 alleles (74.3%) with the IVS-I-5 (G→C) mutation, 12 (15.4%) with the codon 30 (AGG→ACG) mutation, seven (9%) with the IVS-I-1 (G→A) mutation, and one with the codons 41/42 (-TTCT) mutation. The first three mutations account for 98.7% of the total number of β-thalassemia chromosomes studied. These mutations are clustered in the region spanning 6 bp around the junction of exon 1 and the first intervening sequence of the β-globin gene. These observations have significant implications for setting up a thalassemia prevention and control program in the Maldives. Analysis of haplotypes and frameworks of chromosomes bearing each β-thalassemia mutation suggested that the origin and spread of these mutations were reflected by the historical record.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0031897372&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleMolecular basis of β-thalassemia in the Maldivesen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.3109/03630269809092138en_US
Appears in Collections:Scopus 1991-2000

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