Clinical heterogeneity associated with mitochondrial DNA depletion in muscle
- 2 December 1998
- journal article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 8 (8) , 568-573
- https://doi.org/10.1016/s0960-8966(98)00080-7
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in miceNature Genetics, 1998
- Severe myoclonic epilepsy and mitochondrial cytopathyChild's Nervous System, 1997
- Molecular Mechanisms in Mitochondrial DNA Depletion SyndromeHuman Molecular Genetics, 1997
- Mitochondrial DNA depletion: Prevalence in a pediatric population referred for neurologic evaluationPediatric Neurology, 1996
- Mitochondrial defect in Huntington's disease caudate nucleusAnnals of Neurology, 1996
- Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndromePediatric Neurology, 1995
- Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome?Journal of Inherited Metabolic Disease, 1994
- Low Levels of Mitochondrial Transcription Factor A in Mitochondrial DNA DepletionBiochemical and Biophysical Research Communications, 1994
- Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNANeurology, 1992
- Cytochrome c oxidase deficiency in leigh syndromeAnnals of Neurology, 1987