Familial myopathy with conspicuous depletion of mitochondria in muscle fibers: a morphologically distinct disease
- 31 March 1995
- journal article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 5 (2) , 139-144
- https://doi.org/10.1016/0960-8966(94)00039-c
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- In vivo muscle magnetic resonance spectroscopy in the clinical investigation of mitochondria1 diseaseNeurology, 1991
- Bioenergetic heterogeneity of human mitochondrial myopathiesNeurology, 1987
- Investigation of human mitochondrial myopathies by phosphorus magnetic resonance spectroscopyAnnals of Neurology, 1985
- Sequence and organization of the human mitochondrial genomeNature, 1981
- The childhood type of dermatomyositisNeurology, 1976
- The incidence of lobulated fibres in the facioscapulohumeral type of muscular dystrophy and the limb-girdle syndromeJournal of the Neurological Sciences, 1973