Patients with ACVR1R206H mutations have an increased prevalence of cardiac conduction abnormalities on electrocardiogram in a natural history study of Fibrodysplasia Ossificans Progressiva

Overview of attention for article published in Orphanet Journal of Rare Diseases, July 2020

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Kou et al: Patients with ACVR1 R206H mutations have an increased prevalence of cardiac conduction abnormalities on…

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