Acute and crucial requirement for MeCP2 function upon transition from early to late adult stages of brain maturation

Germline mutations in the X-linked gene, methyl-CpG-binding protein 2 (MECP2), underlie most cases of Rett syndrome (RTT), an autism spectrum disorder affecting approximately one in 10 000 female live births. The disease is characterized in affected girls by a latent appearance of symptoms between 1...

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Bibliographic Details
Published in:Hum Mol Genet
Main Authors: Du, Fang, Nguyen, Minh Vu Chuong, Karten, Ariel, Felice, Christy A., Mandel, Gail, Ballas, Nurit
Format: Artigo
Language:Inglês
Published: Oxford University Press 2016
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4986326/
https://ncbi.nlm.nih.gov/pubmed/26908602
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw038
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