The Mutation P.T613a in the Pore Helix of the Kv 11.1 Potassium Channel is Associated with Long Qt Syndrome
Kristian L Poulsen, Mostafa Hotait, Kirstine Calloe, Dan A Klaerke, Abdallah Rebeiz, Georges Nemer, Maria A Tejada, Marwan M Refaat
3Citations
(Scopus)
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