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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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Detalhes bibliográficos
Main Authors: Noutel, Joao, Hong, Y. Kate, Leu, Byunghee, Kang, Erin, Chen, Chinfei
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
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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