Functional role of inward rectifier current in heart probed by Kir2.1 overexpression and dominant-negative suppression
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Reference28 articles.
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2. Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome
3. Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
4. Biological pacemaker created by gene transfer
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