Human primary retinal cells as an in-vitro model for investigating defective signalling caused by OPTN mutants associated with glaucoma
Author:
Funder
Hyderabad Eye Research Foundation
Science and Engineering Research Board
Publisher
Elsevier BV
Subject
Cell Biology,Cellular and Molecular Neuroscience
Reference61 articles.
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3. Clinical features and course of patients with glaucoma with the E50K mutation in the optineurin gene;Aung;Invest. Ophthalmol. Vis. Sci.,2005
4. Variation in optineurin (OPTN) allele frequencies between and within populations;Ayala-Lugo;Mol. Vis.,2007
5. Optineurin promotes autophagosome formation by recruiting the autophagy-related Atg12-5-16L1 complex to phagophores containing the Wipi2 protein;Bansal;J. Biol. Chem.,2018
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