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
Domains
Life Sciences [q-bio]
Origin : Files produced by the author(s)
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