The ciliopathy gene cc2d2a controls zebrafish photoreceptor outer segment development through a role in Rab8-dependent vesicle trafficking

Ciliopathies are a genetically and phenotypically heterogeneous group of human developmental disorders whose root cause is the absence or dysfunction of primary cilia. Joubert syndrome is characterized by a distinctive hindbrain malformation variably associated with retinal dystrophy and cystic kidn...

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Detalles Bibliográficos
Autores principales: Bachmann-Gagescu, Ruxandra, Phelps, Ian G., Stearns, George, Link, Brian A., Brockerhoff, Susan E., Moens, Cecilia B., Doherty, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3177654/
https://www.ncbi.nlm.nih.gov/pubmed/21816947
http://dx.doi.org/10.1093/hmg/ddr332

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3177654/
https://www.ncbi.nlm.nih.gov/pubmed/21816947
http://dx.doi.org/10.1093/hmg/ddr332

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