PCARE requires coiled coil, RP62 kinase-binding and EVH1 domain-binding motifs for ciliary expansion
Tess A. V. Afanasyeva(Radboud University Nijmegen), Rob W.J. Collin(Radboud University Nijmegen)
Cited by 4
Related Papers
Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy
|Nature Genetics|2010|318
Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations
|Progress in Retinal and Eye Research|2020|311
Gene augmentation of LCA5-associated Leber congenital amaurosis ameliorates bulge region defects of the photoreceptor ciliary axoneme
|JCI Insight|2023|25
CRISPR-Cas9 correction of a nonsense mutation in LCA5 rescues lebercilin expression and localization in human retinal organoids
|Molecular Therapy — Methods & Clinical Development|2023|25
Probing the sub-cellular mechanisms of LCA5-Leber Congenital Amaurosis and associated gene therapy with expansion microscopy
|bioRxiv (Cold Spring Harbor Laboratory)|2023|0