CRB1 mutation spectrum in inherited retinal dystrophies. by den Hollander, A, Davis, J, van der Velde-Visser, S, Zonneveld, M, Pierrottet, C, Koenekoop, R, Kellner, U, van den Born, L, Heckenlively, JR, Hoyng, C, Handford, P, Roepman, R, Cremers, F

The natural history of Leber congenital amaurosis and cone–rod dystrophy associated with variants in the GUCY2D gene by Hahn, LC, Georgiou, M, Almushattat, H, van Schooneveld, MJ, de Carvalho, ER, Wesseling, NL, Ten Brink, JB, Florijn, RJ, Lissenberg-Witte, BI, Strubbe, I, van Cauwenbergh, C, de Zaeytijd, J, Walraedt, S, de Baere, E, Mukherjee, R, McKibbin, M, Meester-Smoor, MA, Thiadens, AAHJ, Al-Khuzaei, S, Akyol, E, Lotery, AJ, van Genderen, MM, Norel, JO-V, Ingeborgh van den Born, L, Hoyng, CB, Klaver, CCW, Downes, SM, Bergen, AA, Leroy, BP, Michaelides, M, Boon, CJF