Patients with ACVR1R206H mutations have an increased...

Orphanet Journal of Rare Diseases 2020 / 12 Vol. 15; Iss. 1

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

Kou, Samuel, De Cunto, Carmen, Baujat, Geneviève, Wentworth, Kelly L., Grogan, Donna R., Brown, Matthew A., Di Rocco, Maja, Keen, Richard, Al Mukaddam, Mona, le Quan Sang, Kim-Hanh, Masharani, Umesh,
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Volume:
15
Journal:
Orphanet Journal of Rare Diseases
DOI:
10.1186/s13023-020-01465-x
Date:
December, 2020
File:
PDF, 473 KB
2020
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