Mitochondrial diseases
- 15 June 2004
- journal article
- review article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Bioenergetics
- Vol. 1658 (1-2) , 80-88
- https://doi.org/10.1016/j.bbabio.2004.03.014
Abstract
No abstract availableKeywords
This publication has 61 references indexed in Scilit:
- Effects of Purifying and Adaptive Selection on Regional Variation in Human mtDNAScience, 2004
- Mitochondrial DNA abnormalities and autistic spectrum disordersThe Journal of Pediatrics, 2004
- Mutation Screening in Patients With Isolated Cytochrome c Oxidase DeficiencyPediatric Research, 2003
- Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60American Journal of Human Genetics, 2002
- 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
- Aging, energy, and oxidative stress in neurodegenerative diseasesAnnals of Neurology, 1995
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- Human Myopathy with Giant Abnormal MitochondriaScience, 1964