Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 Gene. [electronic resource]
- Investigative ophthalmology & visual science 05 2017
- 2609-2622 p. digital
Publication Type: Journal Article; Observational Study
1552-5783
10.1167/iovs.17-21560 doi
Adolescent Adult Antigens, Neoplasm--genetics Cell Cycle Proteins Child Child, Preschool Clinical Trials as Topic Cytoskeletal Proteins DNA--genetics DNA Mutational Analysis Electroretinography Female Humans Leber Congenital Amaurosis--diagnosis Male Middle Aged Mutation Neoplasm Proteins--genetics Outcome Assessment, Health Care Retinal Cone Photoreceptor Cells--metabolism Retrospective Studies Tomography, Optical Coherence--methods Young Adult