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The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and management. (2013)

First Author: Nesbitt V

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