Isolated rod dysfunction associated with a novel genotype of CNGB1

بواسطة Ba-Abbad, R., Holder, G.E., Robson, A.G., Neveu, M.M., Waseem, N., Arno, G., Webster, A.R.
منشور في 2021

Clinical features of a retinopathy associated with a dominant allele of the RGR gene

بواسطة Ba-Abbad, R., Leys, M., Wang, X., Chakarova, C., Waseem, N., Carss, K.J., Raymond, F.L., Bujakowska, K.M., Pierce, E.A., Mahroo, O.A., Mohamed, M.D., Holder, G.E., Hummel, M., Arno, G., Webster, A.R.
منشور في 2021

A clinical and molecular characterisation of CRB1-associated maculopathy

بواسطة Khan, K.N, Robson, A, Mahroo, O.A.R, Arno, G, Inglehearn, C.F, Armengol, M, Waseem, N, Holder, G.E, Carss, K.J, Raymond, L.F, Webster, A.R, Moore, A.T, McKibbin, M, Van Genderen, M.M, Poulter, J.A, Michaelides, M
منشور في 2020