Molecular basis of acid ceramidase deficiency in a neonatal form of Farber disease: Identification of the first large deletion in ASAH1 gene

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dc.contributor.author Harzer, Klaus de_DE
dc.date.accessioned 2013-12-03T10:32:42Z
dc.date.available 2013-12-03T10:32:42Z
dc.date.issued 2013 de_DE
dc.identifier.issn 1096-7192 de_DE
dc.identifier.uri http://hdl.handle.net/10900/38557
dc.language.iso en en
dc.publisher Academic Press Inc Elsevier Science de_DE
dc.relation.uri http://dx.doi.org/10.1016/j.ymgme.2013.04.019 de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title Molecular basis of acid ceramidase deficiency in a neonatal form of Farber disease: Identification of the first large deletion in ASAH1 gene de_DE
dc.type Article de_DE
utue.quellen.id 20130911224530_00388 de_DE
utue.publikation.seiten 276-281 de_DE
utue.personen.roh Alves, Mariana Q. de_DE
utue.personen.roh Le Trionnaire, Emmanuelle de_DE
utue.personen.roh Ribeiro, Isaura de_DE
utue.personen.roh Carpentier, Stephane de_DE
utue.personen.roh Harzer, Klaus de_DE
utue.personen.roh Levade, Thierry de_DE
utue.personen.roh Gil Ribeiro, M. de_DE
dcterms.isPartOf.ZSTitelID Molecular Genetics and Metabolism de_DE
dcterms.isPartOf.ZS-Issue 3 de_DE
dcterms.isPartOf.ZS-Volume 109 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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