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Kv1.1 is a voltage-gated potassium channel that plays a critical role in regulating neuronal excitability and action potential repolarization. It is predominantly expressed in the brain and central nervous system, but also found in peripheral nerves and heart tissue. Mutations in the KCNA1 gene, which encodes Kv1.1, can lead to neurological disorders such as episodic ataxia type I and epilepsy. Autoimmune reactions against Kv1.1 can cause Isaacs syndrome. Kv1.1 forms tetrameric channels and its function is influenced by interactions with auxiliary subunits.
Modulation of neuronal excitability through voltage-dependent potassium conductance
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