Ocular phenotype in a mouse gene knockout model for infantile neuronal ceroid lipofuscinosis
Author:
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience
Reference22 articles.
1. Impairment of the Transient Pupillary Light Reflex inRpe65−/−Mice and Humans with Leber Congenital Amaurosis
2. Bright blue times
3. Developmental abnormalities in the Nuc1 rat retina: A spontaneous mutation that affects neuronal and vascular remodeling and retinal function
4. Adeno-associated virus 2-mediated gene therapy decreases autofluorescent storage material and increases brain mass in a murine model of infantile neuronal ceroid lipofuscinosis
5. AAV2-mediated ocular gene therapy for infantile neuronal ceroid lipofuscinosis
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