Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1Frederick S. Kaplan,Meiqi Xu,Petra Seemann,J. Michael Connor,David L. Glaser,Liam Carroll,Patricia Delai,Elisabeth Fastnacht-Urban,Stephen J. Forman,Gabriele Gillessen-Kaesbach,Julie Hoover-Fong,Bernhard Köster,Richard M. Pauli,William Reardon,Syed-Adeel Zaidi,Michael Zasloff,Rolf Morhart,Stefan Mundlos,Jay Groppe,Eileen M. ShoreHuman Mutation（2009）引用 365|浏览19暂无评分AI 理解论文溯源树样例生成溯源树，研究论文发展脉络Chat Paper正在生成论文摘要
