Impaired activity and membrane association of most calpain-5 mutants causal for neovascular inflammatory vitreoretinopathy
Author:
Funder
NINDS
National Institutes of Health
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference98 articles.
1. Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13;Stone;Hum. Mol. Genet.,1992
2. Autosomal dominant neovascular inflammatory vitreoretinopathy;Bennett;Ophthalmology,1990
3. Calpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degeneration;Mahajan;PLoS Genet.,2012
4. Inhibition of neovascularization but not fibrosis with the fluocinolone acetonide implant in autosomal dominant neovascular inflammatory vitreoretinopathy;Tlucek;Arch. Ophthalmol.,2012
5. Surgical management of fibrotic encapsulation of the fluocinolone acetonide implant in CAPN5-associated proliferative vitreoretinopathy;Tlucek;Clin. Ophthalmol.,2013
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