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The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency
- Correspondence to: Dr A Munnich, INSERM U393 and Department of Genetics and Department of Paediatric Radiology, Hôpital Necker-Enfants Malades, 149 rue de Sévres, 75015 Paris, France; munnich{at}necker.fr
Citation
The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency
Publication history
- Accepted November 27, 2002
- Revised November 26, 2002
- First published March 1, 2003.
Online issue publication
April 27, 2016
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Copyright 2003 Journal of Medical Genetics