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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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書誌詳細
主要な著者: Gambino, Frédéric, Khelfaoui, Malik, Poulain, Bernard, Bienvenu, Thierry, Chelly, Jamel, Humeau, Yann
フォーマット: Artigo
言語:Inglês
出版事項: Public Library of Science 2010
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2896423/
https://ncbi.nlm.nih.gov/pubmed/20625482
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0011399
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