Publication:
Molecular basis of β<sup>o</sup>-thalassemia/HbE disease in Thailand

Simple item page
dc.contributor.authorSongsak Petmitren_US
dc.contributor.authorPrapon Wilairaten_US
dc.contributor.authorJiraporn Kownkonen_US
dc.contributor.authorPranee Winichagoonen_US
dc.contributor.authorSuthat Fucharoenen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherFaculty of Medicine, Thammasat Universityen_US
dc.date.accessioned2018-06-14T09:12:51Z
dc.date.available2018-06-14T09:12:51Z
dc.date.issued1989-07-31en_US
dc.description.abstractThe molecular basis of β o -thalassemia/HbE disease in 30 Thai patients was investigated using DNA amplification and dot-blot hybridization with a number of allele specific oligonucleotide probes. The mutations identified were 17 cases of 4 base-pair deletion at codons 41-42, 4 cases of amber mutation at codon 17, and one case each of an ochre mutation at codon 35, a single base substitution at position 5 of IVS-1, and a single base substitution at position 654 of IVS-2. © 1989.en_US
dc.identifier.citationBiochemical and Biophysical Research Communications. Vol.162, No.2 (1989), 846-851en_US
dc.identifier.doi10.1016/0006-291X(89)92387-5en_US
dc.identifier.issn10902104en_US
dc.identifier.issn0006291Xen_US
dc.identifier.other2-s2.0-0024315888en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/15707
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0024315888&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleMolecular basis of β<sup>o</sup>-thalassemia/HbE disease in Thailanden_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0024315888&origin=inwarden_US

Files

Collections

Scopus 1969-1990