Mitochondrial encephalomyopathies: an update
- 1 April 2005
- journal article
- review article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 15 (4) , 276-286
- https://doi.org/10.1016/j.nmd.2004.12.008
Abstract
No abstract availableKeywords
This publication has 102 references indexed in Scilit:
- Parkinsonism, premature menopause, and mitochondrial DNA polymerase γ mutations: clinical and molecular genetic studyThe Lancet, 2004
- Atorvastatin Decreases the Coenzyme Q10 Level in the Blood of Patients at Risk for Cardiovascular Disease and StrokeArchives of Neurology, 2004
- POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletionAnnals of Neurology, 2004
- Effects of Purifying and Adaptive Selection on Regional Variation in Human mtDNAScience, 2004
- Defective Remodeling of Cardiolipin and Phosphatidylglycerol in Barth SyndromeBiochemical and Biophysical Research Communications, 2000
- Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophyNature Genetics, 2000
- OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28Nature Genetics, 2000
- Exercise Intolerance Due to Mutations in the CytochromebGene of Mitochondrial DNANew England Journal of Medicine, 1999
- Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with AminoglycosidesAmerican Journal of Human Genetics, 1998
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988