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

समान संसाधन

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