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

Liknande verk

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