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Co-inheritance of Southeast Asian Ovalocytosis (SAO) and G6PD deficiency associated with acute hemolysis in a Thai patient

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dc.contributor.authorKannadit Prayongratanaen_US
dc.contributor.authorVip Viprakasiten_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.contributor.otherPhramongkutklao College of Medicineen_US
dc.date.accessioned2020-01-27T07:36:44Z
dc.date.available2020-01-27T07:36:44Z
dc.date.issued2019-11-01en_US
dc.identifier.citationBlood Cells, Molecules, and Diseases. Vol.79, (2019)en_US
dc.identifier.doi10.1016/j.bcmd.2019.102347en_US
dc.identifier.issn10960961en_US
dc.identifier.issn10799796en_US
dc.identifier.other2-s2.0-85068929202en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/50045
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85068929202&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleCo-inheritance of Southeast Asian Ovalocytosis (SAO) and G6PD deficiency associated with acute hemolysis in a Thai patienten_US
dc.typeLetteren_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85068929202&origin=inwarden_US

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