Autosomal dominant mutations in POLG and C10orf2: association with late onset chronic progressive external ophthalmoplegia and Parkinsonism in two patients

Reference : Autosomal dominant mutations in POLG and C10orf2: association with late onset chronic...


	Document type :	Scientific journals : Article
	Discipline(s) :	Life sciences : Multidisciplinary, general & others
	To cite this reference:	http://hdl.handle.net/10993/26501

Title :	Autosomal dominant mutations in POLG and C10orf2: association with late onset chronic progressive external ophthalmoplegia and Parkinsonism in two patients
Language :	English
Author, co-author :	Brandon, Barton []
	Diederich, Nico [University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB) > >]
	Soni, Madhu []
	Witte, Katrin []
	Weinhold, Manja []
	Krause, Micaela []
	Jackson, Sandra []
Publication date :	2013
Journal title :	Journal of Neurology
Publisher :	Springer Science & Business Media B.V.
Volume :	260
Pages :	1931–1933
Peer reviewed :	Yes (verified by ORBi^lu)
ISSN :	0340-5354
City :	Darmstadt
Country :	Germany
Research centres :	Luxembourg Centre for Systems Biomedicine (LCSB): Experimental Neurobiology (Balling Group)
Permalink :	http://hdl.handle.net/10993/26501
DOI :	10.1007/s00415-013-6975-2

File(s) associated to this reference

Fulltext file(s):

	File	Commentary	Version	Size	Access
Limited access	Autosomal dominant mutations in POLG and C10orf2 association with late onset chronic progressive external ophthalmoplegia and Parkinsonism in two patients.pdf		Publisher postprint	240.31 kB	Request a copy

All documents in ORBi^lu are protected by a user license.