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Genetic epilepsy caused by CDKL5 gene mutations as an example of epileptic encephalopathy and developmental encephalopathy: literature review and own observations
The disease caused by mutations in the CDKL5 gene (encoding cyclin-dependent kinase 5, CDK5) belongs to the group of early (infantile) epileptic encephalopathies caused by alterations in the genome. Currently, the disease is called “developmental encephalopathy and epileptic encephalopathy type 2”....
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Russo |
| Publicado em: |
ABV-press
2021-07-01
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| Colecção: | Russkij Žurnal Detskoj Nevrologii |
| Assuntos: | |
| Acesso em linha: | https://rjdn.abvpress.ru/jour/article/view/360 |
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