Authors: Procaccio, V Lescuyer, P Bourges, I Beugnot, R Duborjal, H Depetris, D Mousson, B Montfort, MF Smeets, H De Coo, R Issartel, JP

Citation: V. Procaccio et al., Human NDUFS3 gene coding for the 30-kDa subunit of mitochondrial Complex I: genomic organization and expression, MAMM GENOME, 11(9), 2000, pp. 808-810

Authors: Feillet, F Mousson, B Grignon, Y Leonard, JV Vidailhet, M

Citation: F. Feillet et al., Necrotizing encephalopathy and macrocephaly with mitochondrial complex I deficiency, PED NEUROL, 20(4), 1999, pp. 305-308

Authors: Ducluzeau, PH Lachaux, A Bouvier, R Streichenberger, N Stepien, G Mousson, B

Citation: Ph. Ducluzeau et al., Depletion of mitochondrial DNA associated with infantile cholestasis and progressive liver fibrosis, J HEPATOL, 30(1), 1999, pp. 149-155

Authors: Procaccio, V Mousson, B Beugnot, R Duborjal, H Feillet, F Putet, G Pignot-Paintrand, I Lombes, A De Coo, R Smeets, H Lunardi, J Issartel, JP

Citation: V. Procaccio et al., Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts, J CLIN INV, 104(1), 1999, pp. 83-92

Authors: Bonod-Bidaud, C Giraud, S Mandon, G Mousson, B Stepien, G

Citation: C. Bonod-bidaud et al., Quantification of OXPHOS gene transcripts during muscle cell differentiation in patients with mitochondrial myopathies, EXP CELL RE, 246(1), 1999, pp. 91-97