Publication:
Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation: Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine

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dc.contributor.authorsBas, Serpil; Akbarzade, Azad; Atay, Zeynep; Gurbanov, Ziya; Guran, Tulay; Turan, Serap; De Franco, Elisa; Ellard, Sian; Bereket, Abdullah
dc.date.accessioned2022-03-10T17:54:34Z
dc.date.accessioned2026-01-11T08:23:44Z
dc.date.available2022-03-10T17:54:34Z
dc.date.issued2016
dc.identifier.doidoiWOS:000384166800576
dc.identifier.eissn1663-2826
dc.identifier.issn1663-2818
dc.identifier.urihttps://hdl.handle.net/11424/221827
dc.identifier.wosWOS:000384166800576
dc.language.isoeng
dc.publisherKARGER
dc.relation.ispartofHORMONE RESEARCH IN PAEDIATRICS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleThiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation: Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine
dc.typeconferenceObject
dc.type.submeetingabstract
dspace.entity.typePublication
oaire.citation.endPage244
oaire.citation.startPage244
oaire.citation.titleHORMONE RESEARCH IN PAEDIATRICS
oaire.citation.volume86

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