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

Samankaltaisia teoksia

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