Molecular genetics of ocular diseases
Summary:
This paper discusses the molecular genetics of ocular diseases, focusing on retinitis pigmentosa and the identification of disease-causing mutations.
Categories
- Eye health: The paper discusses the molecular genetics of ocular diseases, focusing on the retina and the identification of disease-causing mutations.
- Genetic Disorders: The paper discusses the genetic causes of retinitis pigmentosa, a form of inherited retinal degeneration.
- Cognitive function and memory: The paper discusses the role of the retina in transmitting information for image processing, which is relevant to cognitive function.
Author(s)
G Venturini
Publication Year:
2013
Number of Citations:
0
Related Publications
Eye health
- Phototransduction by retinal ganglion cells that set the circadian clock
- Color appearance models
- Diminished pupillary light reflex at high irradiances in melanopsin-knockout mice
- Strange vision: ganglion cells as circadian photoreceptors
Genetic Disorders
- Genetic reactivation of cone photoreceptors restores visual responses in retinitis pigmentosa
- Drug discovery strategies for inherited retinal degenerations
- The causes of retinal dystrophy and the development of more comprehensive screening approach
- LncRNA-XR_002792574. 1-mediated ceRNA network reveals potential biomarkers in myopia-induced retinal ganglion cell damage