C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.
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P. Coumel | E. Schulze-Bahr | B. Hainque | P. Guicheney | I. Denjoy | C. Donger | K. Schwartz | H. Funke | P. Richard | M. Berthet | H. Hammoude | D. Klug | L. Demay