L. Lasquellec

Retinal dystrophies caused by mutations inRPE65: assessment of visual functions

C. Hamel, B. Arnaud, C. Bazalgette, 2001, The British journal of ophthalmology.

[Molecular genetics of pigmentary retinopathies: identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes].

M. Claustres, C. Bareil, C. Hamel, 2000, Journal francais d'ophtalmologie.

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

J. Grosgeorge, C. Turc‐Carel, G. Lenaers, 2000, Nature Genetics.