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Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/68469
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dc.contributor.authorAdivitch Sripusanapanen_US
dc.contributor.authorArunee Phusuaen_US
dc.contributor.authorKanda Fanhchaksaien_US
dc.contributor.authorPimlak Charoenkwanen_US
dc.date.accessioned2020-04-02T15:27:59Z-
dc.date.available2020-04-02T15:27:59Z-
dc.date.issued2020-04-01en_US
dc.identifier.issn15455017en_US
dc.identifier.issn15455009en_US
dc.identifier.other2-s2.0-85077858678en_US
dc.identifier.other10.1002/pbc.28157en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85077858678&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/68469-
dc.subjectMedicineen_US
dc.titleCompound heterozygosity of a silent beta-thalassemia mutation at the 3′-untranslated region (HBB: c.*132 C>T) and beta-zero thalassemia results in thalassemia intermediaen_US
dc.typeJournalen_US
article.title.sourcetitlePediatric Blood and Canceren_US
article.volume67en_US
article.stream.affiliationsChiang Mai Universityen_US
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