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Corrigendum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva
Shore, Eileen M, Xu, Meiqi, Feldman, George J, Fenstermacher, David A, Brown, Matthew A, Kaplan, Frederick SVolume:
39
Year:
2007
Language:
english
Pages:
1
DOI:
10.1038/ng0207-276b
File:
PDF, 78 KB
english, 2007