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Congenital Hypomyelinating Neuropathy with Lethal Conduction Failure in Mice Carrying the Egr2 I268N Mutation

Mouse models of human disease are helpful for understanding the pathogenesis of the disorder and ultimately for testing potential therapeutic agents. Here, we describe the engineering and characterization of a mouse carrying the I268N mutation in Egr2, observed in patients with recessively inherited...

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Detalhes bibliográficos
Main Authors: Baloh, Robert H., Strickland, Amy, Ryu, Elizabeth, Le, Nam, Fahrner, Timothy, Yang, Mao, Nagarajan, Rakesh, Milbrandt, Jeffrey
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2679588/
https://ncbi.nlm.nih.gov/pubmed/19244508
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.2168-08.2009
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