CRB1 mutation spectrum in inherited retinal dystrophies. nork 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

Mutations in TOPORS cause autosomal dominant retinitis pigmentosa with perivascular retinal pigment epithelium atrophy. nork Chakarova, C, Papaioannou, MG, Khanna, H, Lopez, I, Waseem, N, Shah, A, Theis, T, Friedman, J, Maubaret, C, Bujakowska, K, Veraitch, B, El-Aziz, A, Prescott, D, Parapuram, S, Bickmore, W, Munro, P, Gal, A, Hamel, C, Marigo, V, Ponting, C, Wissinger, B, Zrenner, E, Matter, K, Swaroop, A, Koenekoop, R