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Neuron type-specific loss of CDKL5 leads to alterations in mTOR signaling and synaptic markers
CDKL5 disorder is a devastating neurodevelopmental disorder associated with epilepsy, developmental retardation, autism and related phenotypes. Mutations in the CDKL5 gene, encoding CDKL5, have been identified in this disorder. CDKL5 is a protein with homology to the serine-threonine kinases and inc...
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| Publicat a: | Mol Neurobiol |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6447488/ https://ncbi.nlm.nih.gov/pubmed/30288694 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12035-018-1346-8 |
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