Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5705626 | Ophthalmology | 2016 | 9 Pages |
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.
Keywords
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Authors
Albert MD, Harold MD, Isabelle MD, PhD, Catherine MD, Béatrice PhD, Corinne Baudoin, Moro MD, Martine MD, Benjamin MD, Agnès PhD, Guy PhD, José-Alain MD, Alain MD, Salomon Yves MD, PhD, Christian P. MD, PhD, Isabelle MD, PhD,