International physician survey on management of FOP: a modified Delphi study

Abstract Fibrodysplasia ossificans progressiva (FOP), a disabling disorder of progressive heterotopic ossification (HEO), is caused by heterozygous gain-of- function mutations in Activin receptor A, type I (ACVR1, also known as ALK2), a bone morphogenetic protein (BMP) type I receptor. Presently, sy...

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Main Authors: Maja Di Rocco, Genevieve Baujat, Marta Bertamino, Matthew Brown, Carmen L. De Cunto, Patricia L. R. Delai, Elisabeth M. W. Eekhoff, Nobuhiko Haga, Edward Hsiao, Richard Keen, Rolf Morhart, Robert J. Pignolo, Frederick S. Kaplan
格式: Artigo
語言:Inglês
出版: BMC 2017-06-01
叢編:Orphanet Journal of Rare Diseases
主題:
Fibrodysplasia ossificans progressiva
ACVR1
在線閱讀:http://link.springer.com/article/10.1186/s13023-017-0659-4
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