Mitochondria in neuromuscular disorders
Open Access
- 10 August 1998
- journal article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Bioenergetics
- Vol. 1366 (1-2) , 199-210
- https://doi.org/10.1016/s0005-2728(98)00113-3
Abstract
No abstract availableKeywords
This publication has 64 references indexed in Scilit:
- The Release of Cytochrome c from Mitochondria: A Primary Site for Bcl-2 Regulation of ApoptosisScience, 1997
- A Single Cell Complementation Class is Common to Several Cases of Cytochrome c Oxidase-Defective Leigh's SyndromeHuman Molecular Genetics, 1997
- Complementation analysis of systemic cytochrome oxidase deficiency presenting as Leigh syndromeJournal of Inherited Metabolic Disease, 1996
- Comparative biochemical studies in fibroblasts from patients with different forms of Leigh syndromeJournal of Inherited Metabolic Disease, 1995
- Decreasing hydraulic conductivity of Bruch's membrane: Relevance to photoreceptor survival and lipofuscinosesAmerican Journal of Medical Genetics, 1995
- Mitochondrial carrier proteinsFEBS Letters, 1994
- Low Levels of Mitochondrial Transcription Factor A in Mitochondrial DNA DepletionBiochemical and Biophysical Research Communications, 1994
- A Fatal, Systemic Mitochondrial Disease with Decreased Mitochondrial Enzyme Activities, Abnormal Ultrastructure of the Mitochondria and Deficiency of Heat Shock Protein 60Biochemical and Biophysical Research Communications, 1993
- Mitochondrial Myopathy Caused by Long-Term Zidovudine TherapyNew England Journal of Medicine, 1990
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988