Channelopathies: Kir2.1 mutations jeopardize many cell functions
Author:
Publisher
Elsevier BV
Subject
General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology
Reference14 articles.
1. Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome;Plaster;Cell,2001
2. Inward rectifier potassium channels;Nichols;Annu Rev Physiol,1997
3. The structure of the potassium channel: molecular basis of K+ conduction and selectivity;Doyle;Science,1998
4. Inward rectifiers in the heart: an update on IK1;Lopatin;J Mol Cell Cardiol,2001
5. Role of ER export signals in controlling surface potassium channel numbers;Ma;Science,2001
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