PCARE requires coiled coil, RP62 kinase-binding and EVH1 domain-binding motifs for ciliary expansion

Retinitis pigmentosa (RP) is a genetically heterogeneous form of inherited retinal disease that leads to progressive visual impairment. One genetic subtype of RP, RP54, has been linked to mutations in PCARE (photoreceptor cilium actin regulator). We have recently shown that PCARE recruits WASF3 to t...

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Detalles Bibliográficos
Autores principales: Afanasyeva, Tess A V, Schnellbach, Yan-Ting, Gibson, Toby J, Roepman, Ronald, Collin, Rob W J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9396937/
https://www.ncbi.nlm.nih.gov/pubmed/35253837
http://dx.doi.org/10.1093/hmg/ddac057

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9396937/
https://www.ncbi.nlm.nih.gov/pubmed/35253837
http://dx.doi.org/10.1093/hmg/ddac057

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