Dysfunction of Delayed Rectifier Potassium Channels in an Inherited Cardiac Arrhythmia
Author:
Publisher
Wiley
Subject
History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.1999.tb11302.x/fullpdf
Reference55 articles.
1. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
2. Identification of two new KCNA1 mutations in episodic ataxia/myokymia families
3. Episodic ataxia and myokymia syndrome: A new mutation of potassium channel gene Kv1.1
4. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
5. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
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