Episodic ataxia/myokymia mutations functionally expressed in the Shaker potassium channel
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference31 articles.
1. Episodic ataxia results from voltage-dependent potassium channels with altered functions;Adelman;Neuron,1995
2. A dominantly inherited syndrome with continuous motor neuron discharges;Ashizawa;Ann. Neurol.,1983
3. Functional consequences of potassium channel mutations identified in families with inherited episodic ataxia;Boland;Biophys. Soc. Abstr.,1997
4. Identification of two new KCNA1 mutations in episodic ataxia/myokymia families;Browne;Hum. molec. Genet.,1995
5. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1;Browne;Nat. Genet.,1994
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1. Involvement of the Peripheral Nervous System in Episodic Ataxias;Biomedicines;2020-10-22
2. Distinctive role of KV1.1 subunit in the biology and functions of low threshold K+ channels with implications for neurological disease;Pharmacology & Therapeutics;2016-03
3. The episodic ataxia type 1 mutation I262T alters voltage-dependent gating and disrupts protein biosynthesis of human Kv1.1 potassium channels;Scientific Reports;2016-01-18
4. Peripheral nerve hyperexcitability syndromes;Reviews in the Neurosciences;2015-01-01
5. Episodic Ataxias;Encyclopedia of the Neurological Sciences;2014
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