The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and management. (2013)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1136/jnnp-2012-303528
PubMed Identifier: 23355809
Publication URI: http://europepmc.org/abstract/MED/23355809
Type: Journal Article/Review
Volume: 84
Parent Publication: Journal of neurology, neurosurgery, and psychiatry
Issue: 8
ISSN: 0022-3050