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Localization of retinitis pigmentosa 2 to cilia is regulated by Importin β2
Ciliopathies represent a newly emerging group of human diseases that share a common etiology resulting from dysfunction of the cilium or centrosome. The gene encoding the retinitis pigmentosa 2 protein (RP2) is mutated in X-linked retinitis pigmentosa. RP2 localizes to the ciliary base and this requ...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Company of Biologists
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3039017/ https://ncbi.nlm.nih.gov/pubmed/21285245 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/jcs.070839 |
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