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Functional Invalidation of Putative Sudden Infant Death Syndrome-Associated Variants in the KCNH2-Encoded Kv11.1 Channel.
Smith, Jennifer L; Tester, David J; Hall, Allison R; Burgess, Don E; Hsu, Chun-Chun; Elayi, Samy Claude; Anderson, Corey L; January, Craig T; Luo, Jonathan Z; Hartzel, Dustin N; Mirshahi, Uyenlinh L; Murray, Michael F; Mirshahi, Tooraj; Ackerman, Michael J; Delisle, Brian P.
Afiliación
  • Smith JL; Department of Physiology, Cardiovascular Research Center, Center for Muscle Biology, University of Kentucky, Lexington (J.L.S., A.R.H., D.E.B., B.P.D.).
  • Tester DJ; Departments of Cardiovascular Diseases, Pediatrics, and Molecular Pharmacology & Experimental Therapeutics, Divisions of Heart Rhythm Services and Pediatric Cardiology, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, MN (D.J.T., M.J.A.).
  • Hall AR; Department of Physiology, Cardiovascular Research Center, Center for Muscle Biology, University of Kentucky, Lexington (J.L.S., A.R.H., D.E.B., B.P.D.).
  • Burgess DE; Department of Physiology, Cardiovascular Research Center, Center for Muscle Biology, University of Kentucky, Lexington (J.L.S., A.R.H., D.E.B., B.P.D.).
  • Hsu CC; School of Respiratory Therapy, College of Medicine, Taipei Medical University, Taiwan (C.-C.H.).
  • Elayi SC; University of Kentucky, Gill Heart Institute and VAMC, Cardiology, Lexington (S.C.E.).
  • Anderson CL; Cellular and Molecular Arrhythmias Research Program, Department of Medicine, University of Wisconsin, Madison (C.L.A., C.T.J.).
  • January CT; Cellular and Molecular Arrhythmias Research Program, Department of Medicine, University of Wisconsin, Madison (C.L.A., C.T.J.).
  • Luo JZ; Department of Molecular and Functional Genomics and Genomic Medicine Institute, Geisinger Clinic, Danville, PA (J.Z.L., D.N.H., U.L.M., M.F.M., T.M.).
  • Hartzel DN; Department of Molecular and Functional Genomics and Genomic Medicine Institute, Geisinger Clinic, Danville, PA (J.Z.L., D.N.H., U.L.M., M.F.M., T.M.).
  • Mirshahi UL; Department of Molecular and Functional Genomics and Genomic Medicine Institute, Geisinger Clinic, Danville, PA (J.Z.L., D.N.H., U.L.M., M.F.M., T.M.).
  • Murray MF; Department of Molecular and Functional Genomics and Genomic Medicine Institute, Geisinger Clinic, Danville, PA (J.Z.L., D.N.H., U.L.M., M.F.M., T.M.).
  • Mirshahi T; Department of Molecular and Functional Genomics and Genomic Medicine Institute, Geisinger Clinic, Danville, PA (J.Z.L., D.N.H., U.L.M., M.F.M., T.M.).
  • Ackerman MJ; Departments of Cardiovascular Diseases, Pediatrics, and Molecular Pharmacology & Experimental Therapeutics, Divisions of Heart Rhythm Services and Pediatric Cardiology, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, MN (D.J.T., M.J.A.).
  • Delisle BP; Department of Physiology, Cardiovascular Research Center, Center for Muscle Biology, University of Kentucky, Lexington (J.L.S., A.R.H., D.E.B., B.P.D.). brian.delisle@uky.edu.
Circ Arrhythm Electrophysiol ; 11(5): e005859, 2018 05.
Article en En | MEDLINE | ID: mdl-29752375
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Muerte Súbita del Lactante / Síndrome de QT Prolongado / Mutación Missense / Canal de Potasio ERG1 Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Infant / Male Idioma: En Revista: Circ Arrhythm Electrophysiol Asunto de la revista: ANGIOLOGIA / CARDIOLOGIA Año: 2018 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Muerte Súbita del Lactante / Síndrome de QT Prolongado / Mutación Missense / Canal de Potasio ERG1 Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Infant / Male Idioma: En Revista: Circ Arrhythm Electrophysiol Asunto de la revista: ANGIOLOGIA / CARDIOLOGIA Año: 2018 Tipo del documento: Article