Forward genetic analysis using OCT screening identifies Sfxn3 mutations leading to progressive outer retinal degeneration in mice

Retinal disease and loss of vision can result from any disruption of the complex pathways controlling retinal development and homeostasis. Forward genetics provides an excellent tool to find, in an unbiased manner, genes that are essential to these processes. Using N-ethyl-N-nitrosourea mutagenesis...

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Detalhes bibliográficos
Publicado no:Proc Natl Acad Sci U S A
Main Authors: Chen, Bo, Aredo, Bogale, Ding, Yi, Zhong, Xin, Zhu, Yuanfei, Zhao, Cynthia X., Kumar, Ashwani, Xing, Chao, Gautron, Laurent, Lyon, Stephen, Russell, Jamie, Li, Xiaohong, Tang, Miao, Anderton, Priscilla, Ludwig, Sara, Moresco, Eva Marie Y., Beutler, Bruce, Ufret-Vincenty, Rafael L.
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2020
Assuntos:
Biological Sciences
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7293615/
https://ncbi.nlm.nih.gov/pubmed/32457148
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1921224117
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