A CASE OF LETHAL NEONATAL TYPE CARBAMOYL PHOSPHATE SYNTHETASE 1 DEFICIENCY WITH R233C MUTATION

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dc.contributor.authorUcar, Kalkan S.
dc.contributor.authorBasol, G.
dc.contributor.authorCalkavur, S.
dc.contributor.authorHabif, S.
dc.contributor.authorBayindir, O.
dc.contributor.authorCoker, M.
dc.date.accessioned2019-10-27T21:16:04Z
dc.date.available2019-10-27T21:16:04Z
dc.date.issued2010
dc.departmentEge Üniversitesien_US
dc.identifier.endpageS119en_US
dc.identifier.issn0141-8955
dc.identifier.startpageS119en_US
dc.identifier.urihttps://hdl.handle.net/11454/43620
dc.identifier.volume33en_US
dc.identifier.wosWOS:000281735000368en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofJournal of Inherited Metabolic Diseaseen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleA CASE OF LETHAL NEONATAL TYPE CARBAMOYL PHOSPHATE SYNTHETASE 1 DEFICIENCY WITH R233C MUTATIONen_US
dc.typeConference Objecten_US

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