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 (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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