AN INFANT WITH NOVEL MUTATION OF ALDOLASE A DEFICIENCY PRESENTED WITH NEUROMETABOLIC SIGNS AND BASOPHILIC STRIPPING ON PERIPHERAL BLOOD SMEAR

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dc.contributor.authorÖZCAN ALPER
dc.contributor.authorKADIOĞLU YILMAZ BANU
dc.contributor.authorÜnal, Ekrem
dc.contributor.authorKARDAŞ FATİH
dc.contributor.authorELKATMIŞ TARIK
dc.contributor.authorKUMANDAŞ SEFER
dc.date.accessioned2026-10-15T04:08:01Z
dc.date.issued2020
dc.descriptionUluslararası | Özet bildiri | YÖK-Özgeçmiş
dc.identifier.urihttps://hdl.handle.net/20.500.11782/11035
dc.relation.ispartof25th Congress of the European Hematology Association (EHA25)
dc.relation.urihttps://journals.lww.com/hemasphere/Citation/2020/06001/Abstract_Book__25th_Congress_of_the_European.1.aspx
dc.titleAN INFANT WITH NOVEL MUTATION OF ALDOLASE A DEFICIENCY PRESENTED WITH NEUROMETABOLIC SIGNS AND BASOPHILIC STRIPPING ON PERIPHERAL BLOOD SMEAR
dc.typeConference Object
dspace.entity.typePublication
hku.portal.eseridt:bildiri:1e44b605084e1aa6
hku.yoksis.yayinid6845184
relation.isAuthorOfPublicationcd35ec05-b9b3-4f63-a13f-bc9dc6344971
relation.isAuthorOfPublication.latestForDiscoverycd35ec05-b9b3-4f63-a13f-bc9dc6344971

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