PRPF31 interacts with PRPH2 confirmed by co-immunoprecipitation and co-localization
Author:
Funder
Natural Science Foundation of Guangdong Province
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference13 articles.
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3. Whole exome sequencing reveals novel EYS mutations in Chinese patients with autosomal recessive retinitis pigmentosa;Xiao;Mol. Vis.,2019
4. Whole exome sequencing identifies novel USH2A mutations and confirms Usher syndrome 2 diagnosis in Chinese retinitis pigmentosa patients;Ng;Sci. Rep.,2019
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1. Prph2 knock-in mice recapitulate human central areolar choroidal dystrophy retinal degeneration and exhibit aberrant synaptic remodeling and microglial activation;Cell Death & Disease;2023-11-01
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