Since the discovery of the rhodopsin gene, more than 100 RHO mutations have been identified, accounting for 15% of all types of retinal degeneration, and approximately 25% of autosomal dominant forms of RP.
Studies show that mutations in this gene are responsible for approximately 25% of autosomal dominant forms of RP. Since the discovery of the rhodopsin gene, more than 100 RHO mutations have been identified, accounting for 15% of all types of retinal degeneration.
Since the discovery of the rhodopsin gene, more than 100 RHO mutations have been identified, accounting for 15% of all types of retinal degeneration. Studies show that mutations in this gene are responsible for approximately 25% of autosomal dominant forms of RP.
Since the discovery of the rhodopsin gene, more than 100 RHO mutations have been identified, accounting for 15% of all types of retinal degeneration. Studies show that mutations in this gene are responsible for approximately 25% of autosomal dominant forms of RP.