Cantú Syndrome and Related Disorders

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

Martin Bienengraeber, Timothy M. Olson, Vitaly A. Selivanov et al. · Nature Genetics · 2004 · 377 citations · Full text

Life Sciences, Cardiology, Genetics +12

Spectrum and Prevalence of Mutations Involving BrS1- Through BrS12-Susceptibility Genes in a Cohort of Unrelated Patients Referred for Brugada Syndrome Genetic Testing

Lia Crotti, Cherisse A. Marcou, David J. Tester et al. · Journal of the American College of Cardiology · 2012 · 202 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Dominant missense mutations in ABCC9 cause Cantú syndrome

Magdaléna Harakaľová, J. J. T. van Harssel, Stef van Lieshout et al. · Nature Genetics · 2012 · 200 citations

Life Sciences, Genetics, Molecular Genetics +9

KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillation

Timothy M. Olson, Alexey E. Alekseev, Christophe Moreau et al. · Nature Clinical Practice Cardiovascular Medicine · 2007 · 180 citations · Full text

Medicine, Cardiology, Genetics +14

Cantú Syndrome Is Caused by Mutations in ABCC9

Bregje W.M. van Bon, Christian Gilissen, Dorothy K. Grange et al. · The American Journal of Human Genetics · 2012 · 167 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7