Synaptic Maturation at Cortical Projections to the Lateral Amygdala in a Mouse Model of Rett Syndrome

Rett syndrome (RTT) is a neuro-developmental disorder caused by loss of function of Mecp2 - methyl-CpG-binding protein 2 - an epigenetic factor controlling DNA transcription. In mice, removal of Mecp2 in the forebrain recapitulates most of behavioral deficits found in global Mecp2 deficient mice, in...

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Detalles Bibliográficos
Autores principales: Gambino, Frédéric, Khelfaoui, Malik, Poulain, Bernard, Bienvenu, Thierry, Chelly, Jamel, Humeau, Yann
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896423/
https://www.ncbi.nlm.nih.gov/pubmed/20625482
http://dx.doi.org/10.1371/journal.pone.0011399

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896423/
https://www.ncbi.nlm.nih.gov/pubmed/20625482
http://dx.doi.org/10.1371/journal.pone.0011399

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