Targeting molecular pathways for the treatment of inherited retinal degeneration

Targeting molecular pathways for the treatment of inherited retinal degeneration

Inherited retinal degeneration is a major cause of incurable blindness characterized by loss of retinal photoreceptor cells. Inherited retinal degeneration is characterized by high genetic and phenotypic heterogeneity with several genes mutated in patients affected by these genetic diseases. The hig...

Full description

Bibliographic Details
Main Authors: Meltem Kutluer, Li Huang, Valeria Marigo
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:Neural Regeneration Research
Subjects:
achromatopsia; calcium; calpains; calpastatin; congenital stationary night blindness; leber’s congenital amaurosis; retinitis pigmentosa; stargardt disease
Online Access:http://www.nrronline.org/article.asp?issn=1673-5374;year=2020;volume=15;issue=10;spage=1784;epage=1791;aulast=Kutluer

Internet

http://www.nrronline.org/article.asp?issn=1673-5374;year=2020;volume=15;issue=10;spage=1784;epage=1791;aulast=Kutluer

Similar Items