Complex I deficiency due to loss of Ndufs4 in the brain results in progressive encephalopathy resembling Leigh syndrome
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference33 articles.
1. 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
2. SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY IN AN INFANT
3. Leigh syndrome: Clinical features and biochemical and DNA abnormalities
4. A Single Cell Complementation Class is Common to Several Cases of Cytochrome c Oxidase-Defective Leigh's Syndrome
5. Clinico-neuropathological study of a Chinese case of familial adult Leigh syndrome
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