Cardiolaminopathies from bench to bedside: challenges in clinical decision-making with focus on arrhythmia-related outcomes-Reference-Cited by-同舟云学术

Cardiolaminopathies from bench to bedside: challenges in clinical decision-making with focus on arrhythmia-related outcomes

Published:2018-10-18 Issue:1 Volume:9 Page:442-459
ISSN:1949-1034
Container-title:Nucleus
language:en
Short-container-title:Nucleus

Author:

Boriani Giuseppe¹,Biagini Elena²,Ziacchi Matteo²,Malavasi Vincenzo Livio¹,Vitolo Marco¹,Talarico Marisa¹,Mauro Erminio¹,Gorlato Giulia¹,Lattanzi Giovanna³⁴

Affiliation:

1. Cardiology Division, Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Policlinico di Modena, Modena, Italy

2. Institute of Cardiology, Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, S.Orsola-Malpighi University Hospital, Bologna, Italy

3. CNR Institute of Molecular Genetics, Unit of Bologna, Bologna, Italy

4. Laboratory of Musculoskeletal Cell Biology, Rizzoli Orthopedic Institute, Bologna, Italy

Publisher

Informa UK Limited

Subject

Cell Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/19491034.2018.1506680

Reference78 articles.

1. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

2. Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity

3. Clinical Relevance of Atrial Fibrillation/Flutter, Stroke, Pacemaker Implant, and Heart Failure in Emery-Dreifuss Muscular Dystrophy

4. Current insights intoLMNAcardiomyopathies: Existing models and missing LINCs

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