GPT2 mutations cause developmental encephalopathy with microcephaly and features of complicated hereditary spastic paraplegia

Hengel, H.; Keimer, R.; Deigendesch, W.; Riess, A.; Marzouqa, H.; Zaidan, J.; Bauer, P.; Schoels, L.

dc.contributor.author	Hengel, Holger
dc.contributor.author	Riess, Angelika
dc.contributor.author	Bauer, Peter
dc.contributor.author	Schöls, Ludger
dc.date.accessioned	2019-08-17T11:06:49Z
dc.date.available	2019-08-17T11:06:49Z
dc.date.issued	2018
dc.identifier.issn	1399-0004
dc.identifier.uri	http://hdl.handle.net/10900/91587
dc.language.iso	en	de_DE
dc.publisher	Wiley	de_DE
dc.relation.uri	http://dx.doi.org/10.1111/cge.13390	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	GPT2 mutations cause developmental encephalopathy with microcephaly and features of complicated hereditary spastic paraplegia	de_DE
dc.type	Article	de_DE
utue.quellen.id	20190321153956_01033
utue.publikation.seiten	356-361	de_DE
utue.personen.roh	Hengel, H.
utue.personen.roh	Keimer, R.
utue.personen.roh	Deigendesch, W.
utue.personen.roh	Riess, A.
utue.personen.roh	Marzouqa, H.
utue.personen.roh	Zaidan, J.
utue.personen.roh	Bauer, P.
utue.personen.roh	Schoels, L.
dcterms.isPartOf.ZSTitelID	Clinical Genetics	de_DE
dcterms.isPartOf.ZS-Issue	3-4	de_DE
dcterms.isPartOf.ZS-Volume	94	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE