VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference53 articles.
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3. Differences between familial and sporadic dilated cardiomyopathy: ESC EORP Cardiomyopathy & Myocarditis registry;Asselbergs;ESC Heart Fail,2021
4. A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta;Bjornsson;Eur. Heart J.,2018
5. Assessment of right-sided heart failure in patients with dilated cardiomyopathy using magnetic resonance relaxometry of the liver;Bogaert;Am. J. Cardiol.,2021
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