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CERKL Knockdown Causes Retinal Degeneration in Zebrafish
The human CERKL gene is responsible for common and severe forms of retinal dystrophies. Despite intense in vitro studies at the molecular and cellular level and in vivo analyses of the retina of murine knockout models, CERKL function remains unknown. In this study, we aimed to approach the developme...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Public Library of Science
2013
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3650063/ https://www.ncbi.nlm.nih.gov/pubmed/23671706 http://dx.doi.org/10.1371/journal.pone.0064048 |