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Common KCNH2 Polymorphism (K897T) as a genetic modifier of congenital long QT syndrome

✍ Scribed by Crotti, Lia; Lundquist, Andrew L.; Pedrazzini, Matteo; Insolia, Roberto; Ferrandi, Chiara; De Ferrari, Gaetano M.; Vicentini, Alessandro; Yang, Ping; Landolina, Maurizio; Roden, Dan M.; George, Alfred L.; Schwartz, Peter J.

Book ID: 121996921
Publisher: Elsevier Science
Year: 2005
Tongue: English
Weight: 72 KB
Volume: 2
Category: Article
ISSN: 1547-5271
DOI: 10.1016/j.hrthm.2005.02.344

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