Diagnosis and management of mitochondrial respiratory chain disorders
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference20 articles.
1. Leonard JV, Schapira AH. Mitochondrial respiratory chain disorders I: mitochondrial DNA defects. Lancet 2000; 355: 299–304.
2. Servidei S. Mitochondrial encephalomyopathies:gene mutation. Neuromuscul Disord 2002; 12: 524–529.
3. Leonard JV, Schapira AH. Mitochondrial respiratory chain disorders II: neurodegenerative disorders and nuclear gene defects. Lancet 2000; 355: 389–394.
4. Rotig A, Bourgeron T, Chretien D, Rustin P, Munnich A. Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndrome. Hum Mol Genet 1995; 4: 1327–1330.
5. McShane MA, Hammans SR, Sweeney M et al. Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA. Am J Hum Genet 1991; 48: 39–42.
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