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Investigation of Rett Syndrome using pluripotent stem cells
Rett Syndrome (RTT) is one of most prevalent female neurodevelopmental disorders. De novo mutations in X-linked MECP2 are mostly responsible for RTT. Since the identification of MeCP2 as the underlying cause of RTT, murine models have contributed to understanding the pathophysiology of RTT and funct...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3773984/ https://ncbi.nlm.nih.gov/pubmed/23744605 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcb.24597 |
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