Structural interplay of KV7.1 and KCNE1 is essential for normal repolarization and is compromised in short QT syndrome 2 (KV7.1-A287T)

• Ina Rothenberg, PhD,
• Ilaria Piccini, PhD,
• Eva Wrobel, PhD,
• Birgit Stallmeyer, PhD,
• Jovanca Müller, MD,
• Boris Greber, PhD,
• Nathalie Strutz-Seebohm, PhD,
• Eric Schulze-Bahr, MD,
• Nicole Schmitt, PhD,
• Guiscard Seebohm, PhD

Affiliations

Ina Rothenberg, PhD

Institute for Genetics of Heart Diseases (IfGH), Department of Cardiovascular Medicine, University Hospital Münster, Münster, Germany

Ilaria Piccini, PhD

Institute for Genetics of Heart Diseases (IfGH), Department of Cardiovascular Medicine, University Hospital Münster, Münster, Germany

Eva Wrobel, PhD

Institute for Genetics of Heart Diseases (IfGH), Department of Cardiovascular Medicine, University Hospital Münster, Münster, Germany

Birgit Stallmeyer, PhD

Institute for Genetics of Heart Diseases (IfGH), Department of Cardiovascular Medicine, University Hospital Münster, Münster, Germany

Jovanca Müller, MD

Institute for Genetics of Heart Diseases (IfGH), Department of Cardiovascular Medicine, University Hospital Münster, Münster, Germany

Boris Greber, PhD

Human Stem Cell Pluripotency Laboratory, Max Planck Institute for Molecular Biomedicine, Münster, Germany

Nathalie Strutz-Seebohm, PhD

Institute for Genetics of Heart Diseases (IfGH), Department of Cardiovascular Medicine, University Hospital Münster, Münster, Germany

Eric Schulze-Bahr, MD

Institute for Genetics of Heart Diseases (IfGH), Department of Cardiovascular Medicine, University Hospital Münster, Münster, Germany

Nicole Schmitt, PhD

Danish National Research Foundation Centre for Cardiac Arrhythmia, Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark

Guiscard Seebohm, PhD

Institute for Genetics of Heart Diseases (IfGH), Department of Cardiovascular Medicine, University Hospital Münster, Münster, Germany