A homogenous frameshift mutation in LRAT causes retinitis punctata albescens.A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14.Thr-4-Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch familyMutations in TRPM1 are a common cause of complete congenital stationary night blindness.Autosomal recessive retinitis pigmentosa with preserved para-arteriolar pigment epithelium. First report on familial occurrence
author
type
label
F.C.C. Riemslag