A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference14 articles.
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2. Assessment and therapy monitoring of Leigh disease by MRI and proton spectroscopy;Krägeloh-Mann;Pediatr Neurol,1991
3. Familial Leigh's syndrome. Association with a defect in oxidative metabolism probably restricted to brain;van Erven;J Neurol,1987
4. Sequence and organization of the human mitochondrial genome;Anderson;Nature,1981
5. Detection of extremely low levels of wild-type mitochondrial DNA in the liver of a patient with Pearson syndrome by a sensitive PCR assay;de Vries;J Inherited Metab Dis,1992
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