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Fibrodysplasia Ossificans Progressiva,FOP,Cardiovascular disease,Heterotopic ossification,ECG,Electrocardiogram,Natural history study in FOP
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10.1186/s13023-020-01465-x
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 2020, doi:10.1186/s13023-020-01465-x
Fibrodysplasia Ossificans Progressiva
FOP
Cardiovascular disease
Heterotopic ossification
ECG
Electrocardiogram
Natural history study in FOP
Patients with ACVR1R206H mutations have an increased prevalence of cardiac conduction abnormalities on electrocardiogram in a natural history study of Fibrodysplasia Ossificans Progressiva
Samuel Kou
Carmen De Cunto
Geneviève Baujat
Kelly L. Wentworth
Donna R. Grogan
Matthew A. Brown
Maja Rocco
Richard Keen
Mona Mukaddam
Kim-Hanh Quan Sang
Umesh Masharani
Frederick S. Kaplan
Robert J. Pignolo
Edward C. Hsiao
2020-07-29T10:39:19+02:00
2020-07-29T10:39:19+02:00
2020-07-25T00:21:42+08:00
Arbortext Advanced Print Publisher 9.1.440/W Unicode
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Edward C. Hsiao
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