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