Within the Wellcome Centre for Mitochondrial Research we put patients first and ensure they are at the heart of all that we do. One of the things we value most is our continued relationship with our patients and their supporters and we believe strongly that the whole field will only move forward by us working together. In addition to our research strategy we are very committed to keeping patients and their families fully informed of new advances in mitochondrial research and explaining the complexities of mitochondrial disease. Some of our patient engagement activities and links to further information are shown below:
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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
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