Reply: 'Behr syndrome' with OPA1 compound heterozygote mutations. (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/10.1093/brain/awu235
PubMed Identifier: 25146915
Publication URI: http://europepmc.org/abstract/MED/25146915
Type: Journal Article/Review
Volume: 138
Parent Publication: Brain : a journal of neurology
Issue: Pt 1
ISSN: 0006-8950