Harmonin (Ush1c) is required in zebrafish Müller glial cells for photoreceptor synaptic development and function

Usher syndrome is the most prevalent cause of hereditary deaf-blindness, characterized by congenital sensorineural hearing impairment and progressive photoreceptor degeneration beginning in childhood or adolescence. Diagnosis and management of this disease are complex, and the molecular changes unde...

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Detalles Bibliográficos
Autores principales: Phillips, Jennifer B., Blanco-Sanchez, Bernardo, Lentz, Jennifer J., Tallafuss, Alexandra, Khanobdee, Kornnika, Sampath, Srirangan, Jacobs, Zachary G., Han, Philip F., Mishra, Monalisa, Titus, Tom A., Williams, David S., Keats, Bronya J., Washbourne, Philip, Westerfield, Monte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Limited 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3209648/
https://www.ncbi.nlm.nih.gov/pubmed/21757509
http://dx.doi.org/10.1242/dmm.006429

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3209648/
https://www.ncbi.nlm.nih.gov/pubmed/21757509
http://dx.doi.org/10.1242/dmm.006429

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