Author:
Andrews R M,Griffiths P G,Chinnery P F,Turnbull D M
Publisher
Springer Science and Business Media LLC
Reference25 articles.
1. Chinnery PF, Turnbull DM . Clinical features, investigation, and management of patients with defects of mitochondrial DNA. J Neurol Neurosurg Psychiatry 1997;63:559–63.
2. Newman NJ . Mithochondril diseases and the eye. Ophthalmol Clin North Am 1992;5:405–24.
3. Pavlakis SG, Rowland LP, DeVivo DC, Bonillo E, DiMauro S . Mitochondrial myopathies and encephalomyopathies. In: Plum F, editor. Contemporary neurology. Philadelphia: Davis, 1988:95–133.
4. Fu K, Hartlen R, Johns T, Genge A, Karparti G, Shoubridge EA . A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy. Hum Mol Genet 1996;5:1835–40.
5. Clark K, Bindoff LA, Lightowlers RN, et al. Reversal of a mitochondrial DNA defect in human skeletal muscle. Nature Genet 1997;16:222–4.
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