Article ID Journal Published Year Pages File Type
5705626 Ophthalmology 2016 9 Pages PDF
Abstract
MCRPE is an autosomal dominant, fully penetrant retinal dystrophy with a preclinical stage, an onset after the age of 30 years, and a preserved visual acuity until occurrence of macular complications. The natural history of MCRPE is in relation to the role of MAPKAPK3 in BM modeling, vascular endothelial growth factor activity, retinal pigment epithelial responses to aging, and oxidative stress.
Related Topics
Health Sciences Medicine and Dentistry Ophthalmology
Authors
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