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Microtubules: A Key to Understand and Correct Neuronal Defects in CDKL5 Deficiency Disorder?
CDKL5 deficiency disorder (CDD) is a severe neurodevelopmental encephalopathy caused by mutations in the X-linked CDKL5 gene that encodes a serine/threonine kinase. CDD is characterised by the early onset of seizures and impaired cognitive and motor skills. Loss of CDKL5 in vitro and in vivo affects...
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| Publicado no: | Int J Mol Sci |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6747382/ https://ncbi.nlm.nih.gov/pubmed/31438497 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms20174075 |
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