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

Slični predmeti

• Identification of a novel mutation in activin receptor type 1 (ACVR1) in a fibrodysplasia ossificans progressiva (FOP) patient
  od: Petrie, K, i dr.
  Izdano: (2007)
• Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
  od: Petrie, K, i dr.
  Izdano: (2009)
• Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
  od: Petrie, K, i dr.
  Izdano: (2009)
• Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
  od: Kirsten A Petrie, i dr.
  Izdano: (2009-01-01)
• ACVR1 mutation and Fibrodysplasia Ossificans Progressiva in Chinese children
  od: Ng Bobby KW, i dr.
  Izdano: (2011-09-01)