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KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.
Crotti, Lia; Lundquist, Andrew L; Insolia, Roberto; Pedrazzini, Matteo; Ferrandi, Chiara; De Ferrari, Gaetano M; Vicentini, Alessandro; Yang, Ping; Roden, Dan M; George, Alfred L; Schwartz, Peter J.
Affiliation
  • Crotti L; Department of Cardiology, University of Pavia, IRCCS Policlinico S. Matteo, Pavia, Italy.
Circulation ; 112(9): 1251-8, 2005 Aug 30.
Article in En | MEDLINE | ID: mdl-16116052
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Database: MEDLINE Main subject: Long QT Syndrome / Polymorphism, Single Nucleotide / Ether-A-Go-Go Potassium Channels / Mutation Type of study: Etiology_studies / Prognostic_studies Limits: Adult / Female / Humans Language: En Year: 2005 Type: Article
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PubMed Links

Database: MEDLINE Main subject: Long QT Syndrome / Polymorphism, Single Nucleotide / Ether-A-Go-Go Potassium Channels / Mutation Type of study: Etiology_studies / Prognostic_studies Limits: Adult / Female / Humans Language: En Year: 2005 Type: Article