Kou, S., De Cunto, C., Baujat, G., Wentworth, K. L., Grogan, D. R., Brown, M. A., . . . Hsiao, E. C. (2020). Patients with ACVR1(R206H) mutations have an increased prevalence of cardiac conduction abnormalities on electrocardiogram in a natural history study of Fibrodysplasia Ossificans Progressiva. Orphanet J Rare Dis.
Chicago Style aipamenaKou, Samuel, et al. "Patients With ACVR1(R206H) Mutations Have an Increased Prevalence of Cardiac Conduction Abnormalities On Electrocardiogram in a Natural History Study of Fibrodysplasia Ossificans Progressiva." Orphanet J Rare Dis 2020.
MLA aipamenaKou, Samuel, et al. "Patients With ACVR1(R206H) Mutations Have an Increased Prevalence of Cardiac Conduction Abnormalities On Electrocardiogram in a Natural History Study of Fibrodysplasia Ossificans Progressiva." Orphanet J Rare Dis 2020.