Thr-4-Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family
Published inOphthalmic Genetics
P.T.V.M. de Jong, L.I. van den Born, M.J. van Schooneveld, L.A.M.S. de Jong, F.C.C. Riemslag, A. Gal, E.M. Bleeker-Wagemakers, The order of authors may deviate from the original publication due to temporary technical issues.