Structural modelling of kcnq1 and kcnh2 double mutant proteins, identified in two severe long qt syndrome cases, reveals new insights into cardiac channelopathies
William A. Agudelo, Sebastian Ramiro Gil-Quiñones, Alejandra Fonseca, Alvaro Arenas, Laura Castro, Diana Carolina Sierra-Díaz, Manuel A. Patarroyo, Paul Laissue, Carlos F. Suárez, Rodrigo Cabrera
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