Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia

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dc.contributor.author Schüle-Freyer, Rebecca
dc.date.accessioned 2016-06-16T15:35:37Z
dc.date.available 2016-06-16T15:35:37Z
dc.date.issued 2015
dc.identifier.issn 1537-6605
dc.identifier.uri http://hdl.handle.net/10900/70653
dc.language.iso en de_DE
dc.publisher Cell Press de_DE
dc.relation.uri http://dx.doi.org/10.1016/j.ajhg.2015.10.011 de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia de_DE
dc.type Artikel de_DE
utue.quellen.id 20160427062602_00152
utue.publikation.seiten 855-861 de_DE
utue.personen.roh Schmidt, Wolfgang M.
utue.personen.roh Rutledge, S. Lane
utue.personen.roh Schuele, Rebecca
utue.personen.roh Mayerhofer, Benjamin
utue.personen.roh Zuechner, Stephan
utue.personen.roh Boltshauser, Eugen
utue.personen.roh Bittner, Reginald E.
dcterms.isPartOf.ZSTitelID American Journal of Human Genetics de_DE
dcterms.isPartOf.ZS-Issue 6 de_DE
dcterms.isPartOf.ZS-Volume 97 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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