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Correspondence Arrhythmias in MELAS syndrome

Abstract : With interest we read the article by Thomas et al. about a 44 year old female with MELAS syndrome due to the m.3243ANG mutation, which manifested cardiologically as hypertrophic cardiomyopathy and episodes of supraventricular tachycardia requiring atenolol [1]. We have the following comments and concerns
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Submitted on : Wednesday, February 1, 2017 - 10:18:53 AM
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Josef Finsterer, Sinda Zarrouk-Mahjoub. Correspondence Arrhythmias in MELAS syndrome. Molecular Genetics and Metabolism Reports, Elsevier, 2016, ⟨10.1016/j.ymgmr.2016.03.008⟩. ⟨pasteur-01451418⟩

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