Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death

Genomic Reorganization of Lamin-Associated Domains in Cardiac Myocytes is Associated with Differential Gene Expression and DNA Methylation in Human Dilated Cardiomyopathy

(2019) Sirisha Marreddy Cheedipudi et al.   CIRCULATION RESEARCH

A Novel Truncating LMNA Mutation in Patients with Cardiac Conduction Disorders and Dilated Cardiomyopathy

(2018) Hiroshi Kawakami et al.   International Heart Journal

Genetic basis of cardiomyopathy and the genotypes involved in prognosis and left ventricular reverse remodeling

(2018) Takashige Tobita et al.   Scientific Reports

Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry

(2018) Kenzaburo Nakajima et al.   CIRCULATION JOURNAL

Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation

(2017) Nina Eide Hasselberg et al.   EUROPEAN HEART JOURNAL

Lamin and the heart

(2017) Gabriella Captur et al.   HEART

Gene-Based Risk Stratification for Cardiac Disorders inLMNAMutation CarriersCLINICAL PERSPECTIVE

(2017) Suguru Nishiuchi et al.   Circulation-Cardiovascular Genetics

A novel c.563 T>G, p.L189R lamin A/C mutation in identical twins with dilated cardiomyopathy

(2017) Euijae Lee et al.   KOREAN JOURNAL OF INTERNAL MEDICINE

Long-Term Arrhythmic and Nonarrhythmic Outcomes of Lamin A/C Mutation Carriers

(2016) Saurabh Kumar et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death

(2015) Silvia G. Priori et al.   EUROPEAN HEART JOURNAL

Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations

(2013) Takuro Arimura et al.   CARDIOVASCULAR RESEARCH

Implantable cardioverter-defibrillators in lamin A/C mutation carriers with cardiac conduction disorders

(2013) Frédéric Anselme et al.   HEART RHYTHM

Dilated cardiomyopathy: the complexity of a diverse genetic architecture

(2013) Ray E. Hershberger et al.   Nature Reviews Cardiology

CMR-Verified Interstitial Myocardial Fibrosis as a Marker of Subclinical Cardiac Involvement in LMNA Mutation Carriers

(2013) Marianna Fontana et al.   JACC-Cardiovascular Imaging

Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers

(2012) Ingrid A.W. van Rijsingen et al.   EUROPEAN JOURNAL OF HEART FAILURE

Lamins at a glance

(2012) C. Y. Ho et al.   JOURNAL OF CELL SCIENCE

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

(2012) Ingrid A.W. van Rijsingen et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)

(2011) M. J. Ackerman et al.   EUROPACE

Inherited Cardiomyopathies

(2011) Hugh Watkins et al.   NEW ENGLAND JOURNAL OF MEDICINE

The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy

(2009) Daniel Vega Møller et al.   EUROPEAN JOURNAL OF HEART FAILURE

Lamin A/C Gene and the Heart

(2008) Luisa Mestroni et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY