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...

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Detalles Bibliográficos
Autores principales: Riera, Marina, Burguera, Demian, Garcia-Fernàndez, Jordi, Gonzàlez-Duarte, Roser
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
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

Internet

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

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