Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to L-DOPA treatment. (2013)
Attributed to:
A systematic investigation into the pathogenesis and course of Parkinson's syndrome
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1007/s00415-013-7044-6
PubMed Identifier: 23881105
Publication URI: http://europepmc.org/abstract/MED/23881105
Type: Journal Article/Review
Volume: 260
Parent Publication: Journal of neurology
Issue: 9
ISSN: 0340-5354