Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 (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/awt315
PubMed Identifier: 24253200
Publication URI: http://europepmc.org/abstract/MED/24253200
Type: Journal Article/Review
Parent Publication: Brain
Issue: 1
ISSN: 0006-8950