Skeletal Muscle Involvement in Patients With Truncations of Titin and Familial Dilated Cardiomyopathy
Author:
Funder
Capital Region of Denmark
Rigshospitalet
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference43 articles.
1. Family screening in dilated cardiomyopathy;Vissing;J Am Coll Cardiol HF,2022
2. Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease;Roberts;Sci Transl Med,2015
3. Truncations of titin causing dilated cardiomyopathy;Herman;N Engl J Med,2012
4. Phenotype and clinical outcomes of titin cardiomyopathy;Tayal;J Am Coll Cardiol,2017
5. Dilated cardiomyopathy caused by truncating titin variants: long-term outcomes, arrhythmias, response to treatment and sex differences;Vissing;J Med Genet,2021
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1. Beyond the Beat: Understanding Inherited Risk and Therapeutic Opportunities in Cardiovascular Diseases with Emphasis on Inherited Cardiomyopathies and Inherited Arrhythmic Syndromes;Cardiogenetics;2024-09-02
2. Monoallelic TTN Truncation Variants Identified in Individuals With DCM May Cause a Mild Skeletal Myopathy;JACC: Heart Failure;2024-04
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