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Komen, JC, Thorburn, DR.
Modeling Mitochondrial Dysfunction in Neurodegenerative Disease.
193 -212
2012
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McKenzie, M, Tucker, EJ, Compton, AG, Lazarou, M, George, C, Thorburn, DR, Ryan, MT.
Mutations in the gene encoding C8orf38 block complex I assembly by inhibiting production of the mitochondria-encoded subunit ND1..
J Mol Biol
414(3)
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413 -426
2011
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Hunter, MF, Peters, H, Salemi, R, Thorburn, D, Mackay, MT.
Alpers syndrome with mutations in POLG: clinical and investigative features..
Pediatr Neurol
45(5)
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311 -318
2011
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Menezes, MP, Ryan, MM, Thorburn, D, Christodoulou, JC, North, KN, Ouvrier, RA.
P3.27 Childhood mitochondrial neuropathies: Clinical, electrophysiological and histopathological characteristics.
Neuromuscular Disorders
21(9-10)
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690
2011
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Tucker, EJ, Hershman, SG, Köhrer, C, Belcher-Timme, CA, Patel, J, Goldberger, OA, Christodoulou, J, Silberstein, JM, McKenzie, M, Ryan, MT, et al.
Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation..
Cell Metab
14(3)
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428 -434
2011
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