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Excitatory and inhibitory neuron defects in a mouse model of Scn1b‐linked EIEE52
OBJECTIVE: Human variants in voltage‐gated sodium channel (VGSC) α and β subunit genes are linked to developmental and epileptic encephalopathies (DEEs). Inherited, biallelic, loss‐of‐function variants in SCN1B, encoding the β1/β1B subunits, are linked to early infantile DEE (EIEE52). De novo, monoa...
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| Publicado no: | Ann Clin Transl Neurol |
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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/PMC7664274/ https://ncbi.nlm.nih.gov/pubmed/32979291 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.51205 |
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