SCN5A -: A mechanistic link between inherited cardiomyopathies and a predisposition to arrhythmias?

[1] The long QT syndrome: Ion channel diseases of the heart [J]. MAYO CLINIC PROCEEDINGS, 1998, 73 (03) : 250 - 269

[2] Autosomal dominant dilated cardiomyopathy with atrioventricular block: A lamin A/C defect-related disease [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2002, 39 (06) : 981 - 990

[3] Three-year follow-up of patients with right bundle branch block and ST segment elevation in the right precordial leads - Japanese Registry of Brugada Syndrome [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2001, 37 (07) : 1916 - 1920

[4] Axonal excitability revisited [J]. PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2005, 88 (01) : 59 - 90

[5] Einstein A., 1934, PHILOS SCI, V1, P163, DOI DOI 10.1086/286316

[6] Ellinor Patrick T, 2003, J Cardiovasc Electrophysiol, V14, P1007, DOI 10.1046/j.1540-8167.2003.03307.x

[7] Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (23) : 1715 - 1724

[8] Prevalence of asymptomatic ST segment elevation in right precordial leads with right bundle branch block (Brugada-type ST shift) among the general Japanese population [J]. HEART, 2001, 86 (02) : 161 - 166

[9] Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy [J]. NATURE GENETICS, 2002, 30 (02) : 201 - 204

[10] A QUANTITATIVE DESCRIPTION OF MEMBRANE CURRENT AND ITS APPLICATION TO CONDUCTION AND EXCITATION IN NERVE [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1952, 117 (04): : 500 - 544

[1] The long QT syndrome: Ion channel diseases of the heart [J]. MAYO CLINIC PROCEEDINGS, 1998, 73 (03) : 250 - 269

[2] Autosomal dominant dilated cardiomyopathy with atrioventricular block: A lamin A/C defect-related disease [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2002, 39 (06) : 981 - 990

[3] Three-year follow-up of patients with right bundle branch block and ST segment elevation in the right precordial leads - Japanese Registry of Brugada Syndrome [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2001, 37 (07) : 1916 - 1920

[4] Axonal excitability revisited [J]. PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2005, 88 (01) : 59 - 90

[5] Einstein A., 1934, PHILOS SCI, V1, P163, DOI DOI 10.1086/286316

[6] Ellinor Patrick T, 2003, J Cardiovasc Electrophysiol, V14, P1007, DOI 10.1046/j.1540-8167.2003.03307.x

[7] Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (23) : 1715 - 1724

[8] Prevalence of asymptomatic ST segment elevation in right precordial leads with right bundle branch block (Brugada-type ST shift) among the general Japanese population [J]. HEART, 2001, 86 (02) : 161 - 166

[9] Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy [J]. NATURE GENETICS, 2002, 30 (02) : 201 - 204

[10] A QUANTITATIVE DESCRIPTION OF MEMBRANE CURRENT AND ITS APPLICATION TO CONDUCTION AND EXCITATION IN NERVE [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1952, 117 (04): : 500 - 544