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C2orf71a/pcare1 is important for photoreceptor outer segment morphogenesis and visual function in zebrafish
Mutations in C2orf71 are causative for autosomal recessive retinitis pigmentosa and occasionally cone-rod dystrophy. We have recently discovered that the protein encoded by this gene is important for modulation of the ciliary membrane through the recruitment of an actin assembly module, and have the...
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| Publicado no: | Sci Rep |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6018674/ https://ncbi.nlm.nih.gov/pubmed/29946172 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-27928-7 |
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