A Novel Mitochondrial DNA 8597T>C Mutation of Leigh Syndrome: Report of One Case
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference10 articles.
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2. MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh syndrome): correlation with biochemical defect;Medina;Am J Roentgenol,1990
3. Leigh syndrome: serial MR imaging and clinical follow-up;Arii;Am J Neuroradiol,2000
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