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A novel de novo STXBP1 mutation is associated with mitochondrial complex I deficiency and late-onset juvenile-onset parkinsonism. (2015)

First Author: Keogh MJ

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