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Episodic ataxia type 1 mutations differentially affect neuronal excitability and transmitter release
Heterozygous mutations of KCNA1, the gene encoding potassium channel Kv1.1 subunits, cause episodic ataxia type 1 (EA1), which is characterized by paroxysmal cerebellar incoordination and interictal myokymia. Some mutations are also associated with epilepsy. Although Kv1.1-containing potassium chann...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Company of Biologists Limited
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2773728/ https://ncbi.nlm.nih.gov/pubmed/19779067 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.003582 |
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