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Advances in the pathogenesis of Rett syndrome using cell models
Rett syndrome (RTT) is a progressive neurodevelopmental disorder that occurs mainly in girls with a range of typical symptoms of autism spectrum disorders. MeCP2 protein loss‐of‐function in neural lineage cells is the main cause of RTT pathogenicity. As it is still hard to understand the mechanism o...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773312/ https://www.ncbi.nlm.nih.gov/pubmed/35785421 http://dx.doi.org/10.1002/ame2.12236 |