Ocular gene therapy for choroideremia: clinical trials and future perspectives
Author:
Affiliation:
1. Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neurosciences, University of Oxford & Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK
Funder
Health Innovation Challenge Fund
Publisher
Informa UK Limited
Subject
Optometry,Ophthalmology,Biomedical Engineering
Link
https://www.tandfonline.com/doi/pdf/10.1080/17469899.2018.1475232
Reference69 articles.
1. Cloning of a gene that is rearranged in patients with choroideraemia
2. Retinal Degeneration in Choroideremia: Deficiency of Rab Geranylgeranyl Transferase
3. Cloning and characterization of the human choroideremia gene
4. Molecular basis of choroideremia (CHM): Mutations involving the rab escort protein-1 (REP-1) gene
5. The Spectrum of CHM Gene Mutations in Choroideremia and Their Relationship to Clinical Phenotype
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