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- What are mitochondria?
- About Our Clinic
- General information about mitochondrial disease
- Mitochondrial Reproductive Options
- 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’ syndrome
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- Principal Investigators
- Professor Zofia Chrzanowska-Lightowlers
- Dr Grainne Gorman
- Dr Laura Greaves
- Dr Gavin Hudson
- Professor Mary Herbert
- Professor Robert Lightowlers
- Professor Robert McFarland
- Dr Brendan Payne
- Prof Robert Taylor
- Prof Sir Doug Turnbull
- Dr Tom Nicholls
- Dr Amy Reeve
- Dr Oliver Russell
- Dr Amy Vincent
- Dr Sarah Pickett
- Dr Yi Shiau Ng
- Dr Charlotte Alston
- Post Doctoral Scientists
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- NHS Diagnostic Laboratory Team Members
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We have developed a tool to produce corrected blood and urine m.3243A>G heteroplasmy levels
To access the tool please click on the following link:
