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Results: 4

Authors: Jais, JP Knebelmann, B Giatras, I De Marchi, M Rizzoni, G Renieri, A Weber, M Gross, O Netzer, KO Flinter, F Pirson, Y Verellen, C Wieslander, J Persson, U Tryggvason, K Martin, P Hertz, JM Schroder, C Sanak, M Krejcova, S Carvalho, MF Saus, J Antignac, C Smeets, H Gubler, MC
Citation: Jp. Jais et al., X-linked Alport syndrome: Natural history in 195 families and genotype-phenotype correlations in males, J AM S NEPH, 11(4), 2000, pp. 649-657

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: Rana, M de Coo, I Diaz, F Smeets, H Moraes, CT
Citation: M. Rana et al., An out-of-frame cytochrome b gene deletion from a patient with parkinsonism is associated with impaired complex III assembly and an increase in free radical production, ANN NEUROL, 48(5), 2000, pp. 774-781

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
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