Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele. Issue 7 (1st July 2003) - Perrault, I; Hanein, S; Gerber, S; Barbet, F; Dufier, J-L; Munnich, A; Rozet, J-M; Kaplan, J