Article info
Review
Could it be mitochondrial? When and how to investigate
- Correspondence to: Patrick F Chinnery, Professor of Neurogenetics, Wellcome Trust Senior Fellow in Clinical Science, Mitochondrial Research Group, University of Newcastle upon Tyne & Honorary Consultant Neurologist, Department of Neurology, Regional Neurosciences Centre, Newcastle General Hospital, UK; P.F.Chinnery{at}ncl.ac.uk
Citation
Could it be mitochondrial? When and how to investigate
Publication history
- First published April 12, 2006.
Online issue publication
April 14, 2016
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Copyright 2006 Journal of Neurology Neurosurgery and Psychiatry
Other content recommended for you
- Clinical mitochondrial genetics
- Mitochondrial disease: mimics and chameleons
- Inherited mitochondrial optic neuropathies
- Diagnosis and therapy in neuromuscular disorders: diagnosis and new treatments in mitochondrial diseases
- Mitochondria
- Clinical features, investigation, and management of patients with defects of mitochondrial DNA
- SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletions
- Recognition, investigation and management of mitochondrial disease
- Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies
- Human extraocular muscles in mitochondrial diseases: comparing chronic progressive external ophthalmoplegia with Leber’s hereditary optic neuropathy