Distal myopathy with cachexia: an unrecognised phenotype caused by dominantly-inherited mitochondrial polymerase ? mutations (2013)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1136/jnnp-2012-303232
PubMed Identifier: 22933815
Publication URI: http://europepmc.org/abstract/MED/22933815
Type: Journal Article/Review
Parent Publication: Journal of Neurology, Neurosurgery & Psychiatry
Issue: 1
ISSN: 0022-3050