Two-year progression analysis of RPE65 autosomal dominant retinitis pigmentosa

Retrospective Analysis of Structural Disease Progression in Retinitis Pigmentosa Utilizing Multimodal Imaging

(2017) Thiago Cabral et al.   Scientific Reports

Long-Term Effect of Gene Therapy on Leber’s Congenital Amaurosis

(2015) James W.B. Bainbridge et al.   NEW ENGLAND JOURNAL OF MEDICINE

Three-Year Follow-up after Unilateral Subretinal Delivery of Adeno-Associated Virus in Patients with Leber Congenital Amaurosis Type 2

(2013) Francesco Testa et al.   OPHTHALMOLOGY

A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement

(2011) Sara J Bowne et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Choroideremia: A review of general findings and pathogenesis

(2011) Razek Georges Coussa et al.   OPHTHALMIC GENETICS

Choroideremia: Analysis of the Retina from a Female Symptomatic Carrier

(2008) Vera L. Bonilha et al.   OPHTHALMIC GENETICS