Infantile-onset glycogen storage disease type II: Report of a case presented with lung hypolasia

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dc.contributor.authorCoker, M.
dc.contributor.authorKalkan, S.
dc.contributor.authorKaraplnar, B.
dc.contributor.authorLevent, E.
dc.contributor.authorOzyurek, R.
dc.contributor.authorAtlihan, F.
dc.contributor.authorvan Diggelen, O. P.
dc.contributor.authorGoksen, D.
dc.contributor.authorDarcan, S.
dc.date.accessioned2019-10-27T19:17:43Z
dc.date.available2019-10-27T19:17:43Z
dc.date.issued2006
dc.departmentEge Üniversitesien_US
dc.identifier.endpage123en_US
dc.identifier.issn0141-8955
dc.identifier.startpage123en_US
dc.identifier.urihttps://hdl.handle.net/11454/38459
dc.identifier.volume29en_US
dc.identifier.wosWOS:000240467100464en_US
dc.identifier.wosqualityQ3en_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.titleInfantile-onset glycogen storage disease type II: Report of a case presented with lung hypolasiaen_US
dc.typeConference Objecten_US

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