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dc.contributor.authorSitthichai Panyasaien_US
dc.contributor.authorSakorn Pornpraserten_US
dc.date.accessioned2018-09-05T03:07:32Z-
dc.date.available2018-09-05T03:07:32Z-
dc.date.issued2016-12-01en_US
dc.identifier.issn09740449en_US
dc.identifier.issn09714502en_US
dc.identifier.other2-s2.0-84973637145en_US
dc.identifier.other10.1007/s12288-016-0692-9en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84973637145&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/56000-
dc.description.abstract© 2016, Indian Society of Haematology & Transfusion Medicine. Hemoglobin (Hb) New York [β113 (G15) Val→Glu, GTG>GAG] is a very rare β-chain variant found in Thailand. This variant is often missed by routine laboratory testing because Hb New York and Hb A have the identical retention time on high performance liquid chromatography. We reported here for the first time that the detection of Hb New York in a Thai woman by using capillary electrophoresis (CE). A peak of Hb New York located ahead of Hb A at the electrophoretic zone 11 with a level of 42.8 %. The DNA sequencing revealed the GTG>GAG mutation at codon 113 for Hb New York on one allele of β-globin gene. Therefore, the CE has a high efficiency to prevent the misinterpretation of hemoglobin analysis in patients who are heterozygote of this variant.en_US
dc.subjectMedicineen_US
dc.titleDetection of Hemoglobin New York [β113 (G15) Val→Glu, GTG>GAG] in a Thai Woman by Capillary Electrophoresisen_US
dc.typeJournalen_US
article.title.sourcetitleIndian Journal of Hematology and Blood Transfusionen_US
article.volume32en_US
article.stream.affiliationsUniversity of Phayaoen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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