Ohcanbohtosat - Lombes, A

Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesis. Dahkki Nakase, H, Moraes, C T, Rizzuto, R, Lombes, A, DiMauro, S, Schon, E A

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In vivo functional investigations of lactic acid in patients with respiratory chain disorders Dahkki Touati, G, Rigal, O, Lombes, A, Frachon, P, Giraud, M, de Baulny, H O.

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Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation Dahkki Saada, A, Shaag, A, Arnon, S, Dolfin, T, Miller, C, Fuchs‐Telem, D, Lombes, A, Elpeleg, O

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Neuroferritinopathy in a French family with late onset dominant dystonia Dahkki Chinnery, P, Curtis, A, Fey, C, Coulthard, A, Crompton, D, Curtis, A, Lombes, A, Burn, J

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Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness. Dahkki Manouvrier, S, Rötig, A, Hannebique, G, Gheerbrandt, J D, Royer-Legrain, G, Munnich, A, Parent, M, Grünfeld, J P, Largilliere, C, Lombes, A

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