Expanding the Clinical Phenotype of Emerinopathies

This publication has 7 references indexed in Scilit:

• Cardiac Emerinopathy
  Circulation: Arrhythmia and Electrophysiology, 2020
• A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation
  Nature Communications, 2016
• Atrial arrhythmias in the young: early onset atrial arrhythmias preceding a diagnosis of a primary muscular dystrophy
  EP Europace, 2014
• The structure and function of cardiac t-tubules in health and disease
  Proceedings Of The Royal Society B-Biological Sciences, 2011
• Emerin and the Nuclear Lamina in Muscle and Cardiac Disease
  Circulation Research, 2008
• X‐Linked Nonsyndromic Sinus Node Dysfunction and Atrial Fibrillation Caused by Emerin Mutation
  Journal of Cardiovascular Electrophysiology, 2008
• A Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill
  Circulation Research, 2003