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MeCP2 deficiency disrupts axonal guidance, fasciculation, and targeting by altering Semaphorin 3F function

Rett Syndrome (RTT) is an autism spectrum disorder that results from mutations in the transcriptional regulator methyl-CpG binding protein 2 (MECP2). In the present work, we demonstrate that MeCP2 deficiency disrupts the establishment of neural connections before synaptogenesis. Using both in vitro...

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書誌詳細
主要な著者: Degano, Alicia L., Pasterkamp, Jeroen, Ronnett, Gabriele V.
フォーマット: Artigo
言語:Inglês
出版事項: 2009
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3290450/
https://ncbi.nlm.nih.gov/pubmed/19628041
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mcn.2009.07.009
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