The Mutation P.T613a in the Pore Helix of the Kv11.1 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*

*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

4 Citations (Scopus)

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Biochemistry, Genetics and Molecular Biology

Medicine and Dentistry