Leigh and Leigh-Like Syndrome in Children and Adults
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health
Reference111 articles.
1. Subacute, necrotizing encephalomyelopathy in an infant;Leigh;J Neurol Neurosurg Psychiatry,1951
2. Light and electron microscopy characteristics of the muscle of patients with SURF1 gene mutations associated with Leigh syndrome;Pronicki;J Clin Pathol,2008
3. Long-term outcome of Leigh syndrome caused by the NARP-T8993C mtDNA mutation;Debray;Am J Med Genet [A],2007
4. Defects in energy homeostasis in Leigh syndrome French Canadian variant through PGC-1alpha/LRP130 complex;Cooper;Genes Dev,2006
5. A single cell complementation class is common to several cases of cytochrome c oxidase-defective Leigh's syndrome;Munaro;Hum Mol Genet,1997
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