Report of two FOP cases with 617G>A mutation in the ACVR1 gene from Chinese population

Clin Dysmorphol. 2010 Oct;19(4):206-208. doi: 10.1097/MCD.0b013e32833986c8.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activin Receptors, Type I / genetics*
  • Child, Preschool
  • China
  • Female
  • Humans
  • Male
  • Mutation*
  • Myositis Ossificans / genetics*

Substances

  • ACVR1 protein, human
  • Activin Receptors, Type I