A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia

PURPOSE. The purpose of this study was to identify the molecular basis and characterize the pathological consequences of a spontaneous mutation named cone photoreceptor function loss 8 (cpfl8) in a mouse model with a significantly reduced cone electroretinography (ERG) response. METHODS. The chromos...

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Detalhes bibliográficos
Publicado no:Invest Ophthalmol Vis Sci
Main Authors: Maddox, Dennis M., Collin, Gayle B., Ikeda, Akihiro, Pratt, C. Herbert, Ikeda, Sakae, Johnson, Britt A., Hurd, Ron E., Shopland, Lindsay S., Naggert, Jürgen K., Chang, Bo, Krebs, Mark P., Nishina, Patsy M.
Formato: Artigo
Idioma:Inglês
Publicado em: The Association for Research in Vision and Ophthalmology 2015
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4468423/
https://ncbi.nlm.nih.gov/pubmed/26066746
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.14-16047
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