Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia

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dc.contributor.author Schüle-Freyer, Rebecca
dc.date.accessioned 2013-12-06T09:44:05Z
dc.date.available 2013-12-06T09:44:05Z
dc.date.issued 2013
dc.identifier.issn 0002-9297
dc.identifier.uri http://hdl.handle.net/10900/39052
dc.language.iso en en
dc.publisher Cell Press de_DE
dc.relation.uri http://dx.doi.org/10.1016/j.ajhg.2013.04.018 de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia de_DE
dc.type Artikel de_DE
utue.quellen.id 20130911224530_00502 de_DE
utue.publikation.seiten 965-973 de_DE
utue.personen.roh Oates, Emily C.
utue.personen.roh Rossor, Alexander M.
utue.personen.roh Hafezparast, Majid
utue.personen.roh Gonzalez, Michael
utue.personen.roh Speziani, Fiorella
utue.personen.roh MacArthur, Daniel G.
utue.personen.roh Lek, Monkol
utue.personen.roh Cottenie, Ellen
utue.personen.roh Scoto, Mariacristina
utue.personen.roh Foley, A. Reghan
utue.personen.roh Hurles, Matthew
utue.personen.roh Houlden, Henry
utue.personen.roh Greensmith, Linda
utue.personen.roh Auer-Grumbach, Michaela
utue.personen.roh Pieber, Thomas R.
utue.personen.roh Strom, Tim M.
utue.personen.roh Schule, Rebecca
utue.personen.roh Herrmann, David N.
utue.personen.roh Sowden, Janet E.
utue.personen.roh Acsadi, Gyula
utue.personen.roh Menezes, Manoj P.
utue.personen.roh Clarke, Nigel F.
utue.personen.roh Zuechner, Stephan
utue.personen.roh Muntoni, Francesco
utue.personen.roh North, Kathryn N.
utue.personen.roh Reilly, Mary M.
dcterms.isPartOf.ZSTitelID American Journal of Human Genetics de_DE
dcterms.isPartOf.ZS-Issue 6 de_DE
dcterms.isPartOf.ZS-Volume 92 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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