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ALK2 R206H mutation linked to fibrodysplasia ossificans progressiva confers constitutive activity to the BMP type I receptor and sensitizes mesenchymal cells to BMP-induced osteoblast differentiation and bone formation
Article first published online: 14 DEC 2009
DOI: 10.1359/jbmr.091110
Copyright © 2010 American Society for Bone and Mineral Research
Additional Information
How to Cite
Dinther, M. v., Visser, N., de Gorter, D. J., Doorn, J., Goumans, M.-J., de Boer, J. and ten Dijke, P. (2010), ALK2 R206H mutation linked to fibrodysplasia ossificans progressiva confers constitutive activity to the BMP type I receptor and sensitizes mesenchymal cells to BMP-induced osteoblast differentiation and bone formation. J Bone Miner Res, 25: 1208–1215. doi: 10.1359/jbmr.091110
Publication History
- Issue published online: 27 MAY 2010
- Article first published online: 14 DEC 2009
- Accepted manuscript online: 27 JAN 2010 12:00AM EST
- Manuscript Accepted: 20 NOV 2009
- Manuscript Revised: 12 OCT 2009
- Manuscript Received: 5 AUG 2009
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