articleNature GeneticsApr 23, 2006Closed access

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

EMEileen M. ShoreMXMeiqi XuGFGeorge FeldmanDFDavid FenstermacherTCTae‐Joon Cho

University of Pennsylvania · Seoul National University Children's Hospital · +13 more institutions

PubMed
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Topics
Keywords
  • Fibrodysplasia ossificans progressiva
  • Biology
  • Heterotopic ossification
  • Ossification
  • Genetics
  • Mutation
  • Myositis ossificans
  • Pathology
UN Sustainable Development Goals
  • Partnerships for the goals
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