Variable K + channel subunit dysfunction in inherited mutations of KCNA1
Author:
Affiliation:
1. University Department of Clinical Neurology, Institute of Neurology, UCL, Queen Square, London WC1N 3BG, UK
Publisher
Wiley
Subject
Physiology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1113/jphysiol.2001.013242
Reference40 articles.
1. Episodic ataxia results from voltage-dependent potassium channels with altered functions
2. A Potassium Channel Mutation in Neonatal Human Epilepsy
3. Episodic ataxia/myokymia mutations functionally expressed in the Shaker potassium channel
4. Expression in mammalian cells and electrophysiological characterization of two mutant Kv1.1 channels causing episodic ataxia type 1 (EA-1)
5. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
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