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Reply: 'Behr syndrome' with OPA1 compound heterozygote mutations. (2015)

First Author: Yu-Wai-Man P

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