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Citation: S. Gerber et al., Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis, EUR J HUM G, 9(8), 2001, pp. 561-571

Authors: Rozet, JM Perrault, I Gerber, S Hanein, S Barbet, F Ducroq, D Souied, E Munnich, A Kaplan, J

Citation: Jm. Rozet et al., Complete abolition of the retinal-specific guanylyl cyclase (retGC-1) catalytic ability consistently leads to leber congenital amaurosis (LCA), INV OPHTH V, 42(6), 2001, pp. 1190-1192