Lack of fundus autofluorescence to 488 nanometers from childhood on in patients with early-onset severe retinal dystrophy associated with mutations in RPE65.

Lorenz, Birgit

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] - Ophthalmology Aug 2004 - 1585-94 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0161-6420

10.1016/j.ophtha.2004.01.033 doi


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