Koenekoop,R K

Institution: McGill University Health Centre, Canada

Research Interests: Lead, Retinal, Blindness, Cysts, Disease, Exome, Families, Family, Gene, Genes, Missense Mutation, Mutation, Mutations, Patients, Phenotype, Retinal Disease, Retinitis, Retinitis Pigmentosa, Single Nucleotide Polymorphism, Syndrome