Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Fadi Nasser
Ophthalmic Features of Retinitis Pigmentosa in Cohen Syndrome Caused by Pathogenic Variants in the VPS 13B Gene
Acta Ophthalmologica
Medicine
Ophthalmology
Ophthalmic Features of Cone-Rod Dystrophy Caused by Pathogenic Variants in the ALMS1 Gene
Acta Ophthalmologica
Medicine
Ophthalmology
Related publications
Phenotype-Genotype Correlations in Autosomal Dominant Retinitis Pigmentosa Caused by RHO, D190N
Current Eye Research
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
A Combined in Silico, in Vitro and Clinical Approach to Characterize Novel Pathogenic Missense Variants in PRPF31 in Retinitis Pigmentosa
Frontiers in Genetics
Genetics
Molecular Medicine
Posterior Column Ataxia-Retinitis Pigmentosa Syndrome
Brachydactyly-Short Stature-Retinitis Pigmentosa Syndrome
Retinitis Pigmentosa, Hypertension, and Uraemia in Werner's Syndrome
BMJ
Association of Pathogenic Mutations in TULP1 With Retinitis Pigmentosa in Consanguineous Pakistani Families
Archives of Ophthalmology
Genetic Testing in Patients With Retinitis Pigmentosa: Features of Unsolved Cases
Clinical and Experimental Ophthalmology
Medicine
Ophthalmology
Retinitis Pigmentosa-Intellectual Disability-Deafness-Hypogonadism Syndrome
