- Home
- Our Science Home Page
- Patient And Public
- What are mitochondria?
- About Our Clinic
- General information about mitochondrial disease
- Information for women
- 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
- Our Patient Days
- Mitonews
- Fundraising
- Clinical Professionals
- Clinical Guidelines
- Mitochondrial Patient Cohort
- Engagement
- Team members
- Seminars
- Contact Us
- Euromit 2020
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
