Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1
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S. Mundlos | W. Reardon | R. Pauli | J. Hoover-Fong | J. Connor | M. Zasloff | G. Gillessen‐kaesbach | S. Forman | P. Seemann | F. Kaplan | D. Glaser | J. Groppe | E. Shore | P. Delai | S. Zaidi | L. Carroll | R. Morhart | Meiqi Xu | E. Fastnacht-Urban | B. Köster | G. Gillessen‐Kaesbach