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Results: 1-3 |
Results: 3

Authors: Hamel, CP Griffoin, JM Lasquellec, L Bazalgette, C Arnaud, B
Citation: Cp. Hamel et al., Retinal dystrophies caused by mutations in RPE65: assessment of visual functions, BR J OPHTH, 85(4), 2001, pp. 424-427

Authors: Delettre, C Lenaers, G Griffoin, JM Gigarel, N Lorenzo, C Belenguer, P Pelloquin, L Grosgeorge, J Turc-Carel, C Perret, E Astarie-Dequeker, C Lasquellec, L Arnaud, B Ducommun, B Kaplan, J Hamel, CP
Citation: C. Delettre et al., Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy, NAT GENET, 26(2), 2000, pp. 207-210

Authors: Hamel, CP Griffoin, JM Bazalgette, C Lasquellec, L Duval, PA Bareil, C Beaufrere, L Bonnet, S Eliaou, C Marlhens, F Schmitt-Bernard, CF Tuffery, S Claustres, M Arnaud, B
Citation: Cp. Hamel et al., Molecular genetics of pigmentary retinopathies: Identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes, J FR OPHTAL, 23(10), 2000, pp. 985-995
Risultati: 1-3 |