Publication:
Nondeletional Hb Queens Park [α32(B13)Met→Lys]/Hb H (β4) disease

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dc.contributor.authorSuravee Sroymoraen_US
dc.contributor.authorSumalee Jindadamrongwechen_US
dc.contributor.authorPunnee Butthepen_US
dc.contributor.authorSuporn Chuncharuneeen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherFaculty of Medicine, Ramathibodi Hospital, Mahidol Universityen_US
dc.date.accessioned2018-06-11T04:36:25Z
dc.date.available2018-06-11T04:36:25Z
dc.date.issued2012-06-01en_US
dc.description.abstractA rare nondeletional α-thalassemia-2 (α-thal-2) allele was identified in a Thai boy with Hb H (β4) disease. The proband has α-thal-1 (- SEA type) together with a non productive Hb Queens Park (HBA1:c.98T > A) [α32(B13)Met→Lys] α1-globin variant. No abnormal hemoglobin (Hb) fraction was detected by high performance liquid chromatography (HPLC). The clinical effect of this mutation in the proband was comparable to that of deletional α-thal-2 present in Hb H disease. Copyright © Informa Healthcare USA, Inc.en_US
dc.identifier.citationHemoglobin. Vol.36, No.3 (2012), 293-298en_US
dc.identifier.doi10.3109/03630269.2012.658939en_US
dc.identifier.issn1532432Xen_US
dc.identifier.issn03630269en_US
dc.identifier.other2-s2.0-84860786091en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/13709
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84860786091&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleNondeletional Hb Queens Park [α32(B13)Met→Lys]/Hb H (β4) diseaseen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84860786091&origin=inwarden_US

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