Mapping Pathological Phenotypes in a Mouse Model of CDKL5 Disorder
Mutations in cyclin-dependent kinase-like 5 (CDKL5) cause early-onset epileptic encephalopathy, a neurodevelopmental disorder with similarities to Rett Syndrome. Here we describe the physiological, molecular, and behavioral phenotyping of a Cdkl5 conditional knockout mouse model of CDKL5 disorder. B...
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| Principais autores: | , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Acesso em linha: | https://doi.org/10.1371/journal.pone.0091613 https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0091613&type=printable |
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