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