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Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing

CardiomyopathyUnrelated PatientsCardiac Ryanodine ReceptorMendelian DisorderGenetic DisorderMedicineGeneticsGenetic EpidemiologyMolecular DiagnosticsCardiologyCardiovascular Genetics