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Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6)

By Christian Templin, Jelena-Rima Ghadri, Jean-Sébastien Rougier, Alessandra Baumer, Vladimir Kaplan, Maxime Albesa, Heinrich Sticht, Anita Rauch, Colleen Puleo, Dan Hu, Héctor Barajas-Martinez, Charles Antzelevitch, Thomas F. Lüscher, Hugues Abriel and Firat Duru
Topics: Fasttrack Clinical
Publisher: Oxford University Press
OAI identifier: oai:pubmedcentral.nih.gov:3086900
Provided by: PubMed Central
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