PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia

Ozes, B.; Karagoz, N.; Schuele, R.; Rebelo, A.; Sobrido, M. -J.; Harmuth, F.; Synofzik, M.; Pascual, S. I. P.; Colak, M.; Ciftci-Kavaklioglu, B.; Kara, B.; Ordonez-Ugalde, A.; Quintans, B.; Gonzalez, M. A.; Soysal, A.; Zuchner, S.; Battaloglu, E.

dc.contributor.author	Schüle-Freyer, Rebecca
dc.contributor.author	Harmuth, Florian
dc.contributor.author	Synofzik, Matthis
dc.date.accessioned	2019-04-25T08:21:18Z
dc.date.available	2019-04-25T08:21:18Z
dc.date.issued	2017
dc.identifier.issn	1399-0004
dc.identifier.uri	http://hdl.handle.net/10900/88062
dc.language.iso	en	de_DE
dc.publisher	Wiley	de_DE
dc.relation.uri	http://dx.doi.org/10.1111/cge.13008	de_DE
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia	de_DE
dc.type	Article	de_DE
utue.quellen.id	20190131163842_00614
utue.publikation.seiten	534-539	de_DE
utue.personen.roh	Ozes, B.
utue.personen.roh	Karagoz, N.
utue.personen.roh	Schuele, R.
utue.personen.roh	Rebelo, A.
utue.personen.roh	Sobrido, M. -J.
utue.personen.roh	Harmuth, F.
utue.personen.roh	Synofzik, M.
utue.personen.roh	Pascual, S. I. P.
utue.personen.roh	Colak, M.
utue.personen.roh	Ciftci-Kavaklioglu, B.
utue.personen.roh	Kara, B.
utue.personen.roh	Ordonez-Ugalde, A.
utue.personen.roh	Quintans, B.
utue.personen.roh	Gonzalez, M. A.
utue.personen.roh	Soysal, A.
utue.personen.roh	Zuchner, S.
utue.personen.roh	Battaloglu, E.
dcterms.isPartOf.ZSTitelID	Clinical Genetics	de_DE
dcterms.isPartOf.ZS-Issue	5	de_DE
dcterms.isPartOf.ZS-Volume	92	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE