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Harmonin (Ush1c) is required in zebrafish Müller glial cells for photoreceptor synaptic development and function
SUMMARY 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 chan...
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| Main Authors: | , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Company of Biologists
2011-11-01
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| Colecção: | Disease Models & Mechanisms |
| Acesso em linha: | http://dmm.biologists.org/content/4/6/786 |
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