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Therapeutic Potential of Transcranial Focused Ultrasound for Rett Syndrome
Rett syndrome (RTT) is a severe neurodevelopmental disorder occurring almost exclusively in females and is caused by loss-of-function mutations in the gene encoding methyl-CpG-binding protein 2 (MeCP2) in the majority of cases. MeCP2 is essential for the normal function of nerve cells, including neu...
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| Publicado en: | Med Sci Monit |
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| Autor Principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
International Scientific Literature, Inc.
2016
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5087669/ https://ncbi.nlm.nih.gov/pubmed/27786169 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12659/MSM.898041 |
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