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Reversal of phenotypes in MECP2 duplication mice using genetic rescue or antisense oligos

Copy number variations have been frequently associated with developmental delay, intellectual disability, and autism spectrum disorders(1). MECP2 duplication syndrome is one of the most common genomic rearrangements in males(2) and is characterized by autism, intellectual disability, motor dysfuncti...

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Detalhes bibliográficos
Publicado no:Nature
Principais autores: Sztainberg, Yehezkel, Chen, Hong-mei, Swann, John W., Hao, Shuang, Tang, Bin, Wu, Zhenyu, Tang, Jianrong, Wan, Ying-Wooi, Liu, Zhandong, Rigo, Frank, Zoghbi, Huda Y.
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4839300/
https://ncbi.nlm.nih.gov/pubmed/26605526
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature16159
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