Novel homogentisate dioxigenase (HGD) gene mutations in alkaptonuria patients

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dc.contributor.authorHatipoglu, E.
dc.contributor.authorOzgul, R. K.
dc.contributor.authorSivri, H. S.
dc.contributor.authorCoskun, T.
dc.contributor.authorTokatli, A.
dc.contributor.authorKaraca, Şefayet
dc.contributor.authorKucuk, O.
dc.contributor.authorKilic, M.
dc.contributor.authorAkcelik, M.
dc.contributor.authorDursun, A.
dc.date.accessioned13.07.201910:50:10
dc.date.accessioned2019-07-16T09:20:28Z
dc.date.available13.07.201910:50:10
dc.date.available2019-07-16T09:20:28Z
dc.date.issued2010
dc.departmentSağlık Bilimleri Fakültesi
dc.description.abstract[Abstract Not Available]
dc.identifier.endpageS43en_US
dc.identifier.issn0141-8955
dc.identifier.startpageS43en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12451/5093
dc.identifier.volume33en_US
dc.identifier.wosWOS:000281735000092
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.publisherSpringer
dc.relation.ispartofJournal of Inherited Metabolic Disease
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleNovel homogentisate dioxigenase (HGD) gene mutations in alkaptonuria patients
dc.typeConference Object

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