An atypical mutation in the activin a receptor, type 1 gene (ACVR1) in a severely affected Fibrodysplasia Ossificans Progressiva patient

مواد مشابهة

• Identification of a novel mutation in activin receptor type 1 (ACVR1) in a fibrodysplasia ossificans progressiva (FOP) patient
  حسب: Petrie, K, وآخرون
  منشور في: (2007)
• Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
  حسب: Petrie, K, وآخرون
  منشور في: (2009)
• Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
  حسب: Petrie, K, وآخرون
  منشور في: (2009)
• ACVR1 mutation and Fibrodysplasia Ossificans Progressiva in Chinese children
  حسب: Ng Bobby KW, وآخرون
  منشور في: (2011-09-01)
• Mutation Detection in Activin A Receptor, Type I (ACVR1) Gene in Fibrodysplasia Ossificans Progressiva in An Iranian Family
  حسب: Ziba Morovvati, وآخرون
  منشور في: (2014-03-01)