Ophthalmological manifestations in patients with Leigh syndrome
Author:
Publisher
BMJ
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Reference23 articles.
1. Subacute necrotizing encephalomyelopathy in an infant;Leigh;J Neurol Neurosurg Psychiatry,1951
2. Leigh and Leigh-like syndrome in children and adults;Finsterer;Pediatr Neurol,2008
3. Leigh syndrome: clinical features and biochemical and DNA abnormalities;Rahman;Ann Neurol,1996
4. A single cell complementation class is common to several cases of cytochrome c oxidase-defective Leigh's syndrome;Munaro;Hum Mol Genet,1997
5. 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;Chol;J Med Genet,2003
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