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Publications by Dror Sharon
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
American Journal of Human Genetics
Genetics
Variable Retinal Phenotypes Caused by Mutations in the X-Linked Photopigment Gene Array
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Exome Sequencing Identifies a Founder Frameshift Mutation in an Alternative Exon of USH1C as the Cause of Autosomal Recessive Retinitis Pigmentosa With Late-Onset Hearing Loss
PLoS ONE
Multidisciplinary
Association of Pattern Dystrophy With an HTRA1 Single-Nucleotide Polymorphism
Archives of Ophthalmology
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