(Q28265302)

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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

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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 (English)
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Maarten van Dinther
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Nils Visser
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David J J de Gorter
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Joyce Doorn
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Marie-José Goumans
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Jan de Boer
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Peter ten Dijke
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June 2010
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25
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6
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1208-15
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