Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 Gene. [electronic resource]
Producer: 20170719Description: 2609-2622 p. digitalISSN:- 1552-5783
- 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
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Publication Type: Journal Article; Observational Study
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