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- What are mitochondria?
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- General information about mitochondrial disease
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- Specific conditions
- Large-scale mitochondrial DNA deletions
- Neurogenic weakness, Ataxia, and Retinitis Pigmentosa (NARP)
- Multiple mitochondrial DNA deletions
- Mitochondrial Neuro-gastro-intestinal encephalopathy (MNGIE)
- Myoclonic Epilepsy and Ragged Red Fibres (MERRF 8344 A>G)
- Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS) 3243 A>G mutation
- Leigh syndrome
- Mitochondrial DNA depletion syndrome (MDDS)
- Alpers disease
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We have developed a tool to forecast m.3243A>G heteroplasmy levels in children
To access the tool please click on the following link: forecast m.3243A>G heteroplasmy levels in children