Lack of fundus autofluorescence to 488 nanometers from childhood on in patients with early-onset severe retinal dystrophy associated with mutations in RPE65. [electronic resource]
Producer: 20040810Description: 1585-94 p. digitalISSN:- 0161-6420
- Adolescent
- Adult
- Biomarkers
- Carrier Proteins
- Child
- Eye Proteins
- Female
- Fluorescence
- Fundus Oculi
- Genotype
- Humans
- Lasers
- Lipofuscin -- metabolism
- Male
- Middle Aged
- Mutation
- Ophthalmoscopes
- Pigment Epithelium of Eye -- metabolism
- Proteins -- genetics
- Pyridinium Compounds -- metabolism
- Retinal Degeneration -- genetics
- Retinoids -- metabolism
- Tomography, Optical Coherence
- cis-trans-Isomerases
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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