A coincidence of mucopolysaccharidosis type IIIA and familial hypercholesterolaemia type II A: A case report

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dc.contributor.authorKalkan, S.
dc.contributor.authorCoker, M.
dc.contributor.authorvan Diggelen, O. P.
dc.contributor.authorHuijmans, J.
dc.contributor.authorGoksen, D.
dc.contributor.authorDarcan, S.
dc.date.accessioned2019-10-27T19:17:44Z
dc.date.available2019-10-27T19:17:44Z
dc.date.issued2006
dc.departmentEge Üniversitesien_US
dc.identifier.endpage150en_US
dc.identifier.issn0141-8955
dc.identifier.startpage150en_US
dc.identifier.urihttps://hdl.handle.net/11454/38462
dc.identifier.volume29en_US
dc.identifier.wosWOS:000240467100572en_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.titleA coincidence of mucopolysaccharidosis type IIIA and familial hypercholesterolaemia type II A: A case reporten_US
dc.typeConference Objecten_US

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