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Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches
Kv1.1 belongs to the Shaker subfamily of voltage-gated potassium channels and acts as a critical regulator of neuronal excitability in the central and peripheral nervous systems. KCNA1 is the only gene that has been associated with episodic ataxia type 1 (EA1), an autosomal dominant disorder charact...
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| Vydáno v: | Int J Mol Sci |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
MDPI
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7215777/ https://ncbi.nlm.nih.gov/pubmed/32331416 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21082935 |
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