Rare coding variants in MYH6 are associated with atrial fibrillation: results from 45,596 exomes representing the general population von Vad, O.B, Paludan-Muller, C, Ahlberg, G, Andreasen, L, Refsgaard, L, Lundegaard, P.R, Haunso, S, Svendsen, J.H, Olesen, M.S

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Rare variants in HCN4 identified in the general population are associated with complete atrioventricular (AV) block, 1. degree AV block and bundle branch block, results from 50.000... von Jensen, J, Vad, O.B, Paludan-Muller, C, Lundegaard, P.R, Svendsen, J.H, Haunsoe, S, Bundgaard, H, Olesen, M.S

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Supplementary Material for: PKD Phosphorylation as Novel Pathway of KV11.1 Regulation von Steffensen, A.B., Bomholtz, S.H., Andersen, M.N., Olsen, J.V., Mutsaers, N., Lundegaard, P.R., Lundby, A., Schmitt, N.

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