Multiomic Analyses Reveal Brainstem Metabolic Changes in a Mouse Model of Dravet Syndrome
Dravet Syndrome (DS) is a severe genetic epileptic encephalopathy caused by mutations in the <i>SCN1A</i> gene that encodes the voltage-gated sodium channel (Na<sub>V</sub>1.1) subunit alpha. DS is characterized by intractable seizures, progressive developmental delay, cognitive impairment, and high...
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| Principais autores: | , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
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MDPI AG
2025-12-01
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| Colecção: | Cells |
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| Acesso em linha: | https://www.mdpi.com/2073-4409/15/1/67 |
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