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Gabra2 is a genetic modifier of Scn8a encephalopathy in the mouse*
OBJECTIVE: SCN8A encephalopathy is a developmental epileptic encephalopathy typically caused by de novo gain‐of‐function mutations in Na(v)1.6. Severely affected individuals exhibit refractory seizures, developmental delay, cognitive disabilities, movement disorders, and elevated risk of sudden deat...
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| Publicado no: | Epilepsia |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7756374/ https://ncbi.nlm.nih.gov/pubmed/33140451 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/epi.16741 |
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