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Moreover, mutations TXNRD2 have been reported to cause DCM [75, 76], while specific single-nucleotide polymorphisms (SNPs) can predispose patients to a higher risk of myocardial infarction [77]

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Bjarnason NH, Henriksen EE, Alexandersen P, et al

What type of treatment is available

2022 AHA/ACC/HFSA guideline for the management of heart failure: executive summary: a report of the American College of cardiology/American heart association joint committee on clinical practice guidelines