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EHMT1 regulates Parvalbumin-positive interneuron development and GABAergic input in sensory cortical areas
Mutations in the Euchromatic Histone Methyltransferase 1 (EHMT1) gene cause Kleefstra syndrome, a rare form of intellectual disability (ID) with strong autistic traits and sensory processing deficits. Proper development of inhibitory interneurons is crucial for sensory function. Here we report a tim...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer Berlin Heidelberg
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674571/ https://www.ncbi.nlm.nih.gov/pubmed/32975655 http://dx.doi.org/10.1007/s00429-020-02149-9 |