Novel molecular mechanisms for Prph2‐associated pattern dystrophy
Author:
Affiliation:
1. Department of Biomedical Engineering University of Houston Houston TX USA
2. Department of Cell Biology University of Oklahoma Health Sciences Center Oklahoma City OK USA
Publisher
Wiley
Subject
Genetics,Molecular Biology,Biochemistry,Biotechnology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.201901888R
Reference64 articles.
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2. Rom1 converts Y141C‐Prph2‐associated pattern dystrophy to retinitis pigmentosa;Conley SM;Hum Mol Genet,2017
3. Autosomal dominant retinal dystrophies caused by a founder splice site mutation, c.828+3A>T, in PRPH2 and protein haplotypes in trans as modifiers;Shankar SP;Invest Ophthalmol Vis Sci,2016
4. ABCA4andROM1:Implications for Modification of thePRPH2-Associated Macular Dystrophy Phenotype
5. The effect of peripherin/rds haploinsufficiency on rod and cone photoreceptors;Cheng T;J Neurosci,1997
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