Mutation of Mitochondrial DNA G13513A Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference20 articles.
1. Mitochondrial cytopathies;Schmiedel;J Neurol,2003
2. 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
3. Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS;Santorelli;Biochem Biophys Res Commun,1997
4. Clinical and molecular findings in children with complex I deficiency;Bugiani;Biochim Biophys Acta,2004
5. Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's disease;Kirby;Ann Neurol,2003
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