KCNH2 MUTATIONS THAT ALTER KV11.1 CHANNEL GATING ARE LINKED TO SUDDEN INFANT DEATH SYNDROME von Smith, J.L, Tester, D.J, Reloj, A.R, Burgess, D.E, Hsu, C, Ackerman, M.J, Delisle, B.P

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Protracted QTc Prolongation following Treadmill Testing Identifies a Type 1 Long QT Mutation that is Resistant to PKA Activation von Bartos, D.C, Giudicessi, J, Tester, D.J, Ackerman, M.J, Delisle, B.P

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Atomic-Scale Modeling Predicts a Mechanism for Long QT Type 1 Dysfunction Associated With Pore Mutations von Burgess, D.E, Bartos, D.C, Schmidt, E.S, Johnson, J.N, Tester, D.J, Ohno, S, Horie, M, Ackerman, M.J, Delisle, B.P

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2014-A-30-CES - KCNH2 MUTATIONS THAT ALTER KV11.1 CHANNEL GATING ARE LINKED TO SUDDEN INFANT DEATH SYNDROME von Smith, J.L., Tester, D.J., Reloj, A.R., Burgess, D.E., Hsu, C., Ackerman, M.J., Delisle, B.P.

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LUF7244 plus Dofetilide Rescues Aberrant Kv11.1 Trafficking and Produces Functional IKv11.1 von Qile, M., Ji, Y., Golden, T.D., Houtman, M.J.C., Romunde, F., Fransen, D., Ham, W.B. van, IJzerman, A.P., January, C.T., Heitman, L.H., Stary-Weinzinger, A., Delisle, B.P., Heyden, M.A.G. van der

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