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Experience-Dependent Retinogeniculate Synapse Remodeling is Abnormal in MeCP2 deficient mice
Mutations in MECP2 underlie the neurodevelopmental disorder Rett (RTT) syndrome. One hallmark of RTT is relatively normal development followed by a later onset of symptoms. Growing evidence suggests an etiology of disrupted synaptic function, yet it is unclear how these abnormalities explain the cli...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3082316/ https://ncbi.nlm.nih.gov/pubmed/21482354 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuron.2011.03.001 |
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