Autosomal dominant mutations in POLG and C10orf2: association with late onset chronic progressive external ophthalmoplegia and Parkinsonism in two patients
Autosomal dominant mutations in POLG and C10orf2 association with late onset chronic progressive external ophthalmoplegia and Parkinsonism in two patients.pdf
Luxembourg Centre for Systems Biomedicine (LCSB): Experimental Neurobiology (Balling Group)
Disciplines :
Life sciences: Multidisciplinary, general & others
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
External co-authors :
yes
Language :
English
Title :
Autosomal dominant mutations in POLG and C10orf2: association with late onset chronic progressive external ophthalmoplegia and Parkinsonism in two patients
Publication date :
2013
Journal title :
Journal of Neurology
ISSN :
0340-5354
eISSN :
1432-1459
Publisher :
Springer Science & Business Media B.V., Darmstadt, Germany
