A novel de novo STXBP1 mutation is associated with mitochondrial complex I deficiency and late-onset juvenile-onset parkinsonism. (2015)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1007/s10048-014-0431-z
PubMed Identifier: 25418441
Publication URI: http://europepmc.org/abstract/MED/25418441
Type: Journal Article/Review
Volume: 16
Parent Publication: Neurogenetics
Issue: 1
ISSN: 1364-6745