Treatment Potential for Macular Cone Vision in Leber Congenital Amaurosis Due to CEP290 or NPHP5 Mutations: Predictions From Artificial Intelligence. [electronic resource]
Producer: 20191206Description: 2551-2562 p. digitalISSN:- 1552-5783
- Adolescent
- Adult
- Antigens, Neoplasm -- genetics
- Calmodulin-Binding Proteins -- genetics
- Cell Cycle Proteins
- Color Vision Defects -- genetics
- Cytoskeletal Proteins
- Female
- Genetic Therapy
- Humans
- Leber Congenital Amaurosis -- genetics
- Machine Learning
- Male
- Middle Aged
- Mutation
- Neoplasm Proteins -- genetics
- Retinal Cone Photoreceptor Cells -- physiology
- Retinitis Pigmentosa -- genetics
- Tomography, Optical Coherence -- methods
- Visual Field Tests
- Visual Fields -- physiology
- Young Adult
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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