Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1. (2014)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/brain/awu187
PubMed Identifier: 25012222
Publication URI: http://europepmc.org/abstract/MED/25012222
Type: Journal Article/Review
Volume: 137
Parent Publication: Brain : a journal of neurology
Issue: Pt 10
ISSN: 0006-8950