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
Authors:
Raison-Peyron, N
Duval, PA
Barneon, G
Durand, L
Arnaud, B
Meynadier, J
Hamel, C
Citation: N. Raison-peyron et al., A syndrome combining severe hypotrichosis and macular dystrophy: absence of mutations in TIMP genes, BR J DERM, 143(4), 2000, pp. 902-904