From the contents Genetic Factors Modifying Clinical Expression of Autosomal Dominant Rp -- Disease-Associated Variants of The Rod-Derived Cone Viability Factor (Rdcvf) In Leber Congenital Amaurosis. Rod-Derived Cone Viability Variants in Lca -- Leber Congenital Amaurosis: Survey of The Genetic Heterogeneity, Refinement of The Clinical Definition and Phenotype-Genotype Correlations as A Strategy For Molecular Diagnosis. Clinical and Molecular Survey in Lca -- A First Locus For Isolated Autosomal Recessive Optic Atrophy (Roa1) Maps To Chromosome 8q21-Q22 -- Rcc1-Like Domain and ORF15: Essentials in Rpgr Gene -- Choroidal Neovascularization in Patients with Adult-Onset Foveomacular Dystrophy Caused by Mutations in the Rds/Peripherin Gene -- Biochemical Characterisation of the C1QTNF5 Gene Associated With Late-Onset Retinal Degeneration. A Genetic Model of Age-Related Macular Degeneration -- Bietti Crystalline Corneoretinal Dystrophy Associated with Cyp4v2 Gene Mutations -- Fundus Appearance Of Choroideremia Using Optical Coherence Tomograpy -- A2e, A Fluorophore Of Rpe Lipofuscin, Can Destabilie Membrane -- Amino-Retinoid Compounds in The Human Retinal Pigment Epithelium -- Annexins In Bruch’s Membrane and Drusen -- Molecular Mechanisms of Photoreceptor Degeneration in RP Caused by Impdh1 Mutations.