A rare homozygous microdeletion syndrome: hypotonia-cystinuria syndrome

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dc.contributor.authorMetli, Kubra
dc.contributor.authorZamani, Ayse
dc.contributor.authorOzdemir, Taha
dc.contributor.authorYildirim, M. Selman
dc.date.accessioned2024-02-23T14:49:26Z
dc.date.available2024-02-23T14:49:26Z
dc.date.issued2021
dc.departmentNEÜen_US
dc.description.abstract[Abstract Not Availabe]en_US
dc.identifier.endpageS120en_US
dc.identifier.issn1096-7192
dc.identifier.issn1096-7206
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpageS120en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12452/18173
dc.identifier.volume132en_US
dc.identifier.wosWOS:000639219800180en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherAcademic Press Inc Elsevier Scienceen_US
dc.relation.ispartofMolecular Genetics And Metabolismen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[Keyword Not Available]en_US
dc.titleA rare homozygous microdeletion syndrome: hypotonia-cystinuria syndromeen_US
dc.typeConference Objecten_US

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