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

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

書目詳細資料
Main Authors: Petrie, K, Pointon, J, Smith, R, Russell, R, Wordsworth, P, Triffitt, J
格式: Conference item
出版: 2007
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  • Identification of a novel mutation in activin receptor type 1 (ACVR1) in a fibrodysplasia ossificans progressiva (FOP) patient
    由: Petrie, K, et al.
    出版: (2007)
  • Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
    由: Petrie, K, et al.
    出版: (2009)
  • Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
    由: Petrie, K, et al.
    出版: (2009)
  • ACVR1 mutation and Fibrodysplasia Ossificans Progressiva in Chinese children
    由: Ng Bobby KW, et al.
    出版: (2011-09-01)
  • Mutation Detection in Activin A Receptor, Type I (ACVR1) Gene in Fibrodysplasia Ossificans Progressiva in An Iranian Family
    由: Ziba Morovvati, et al.
    出版: (2014-03-01)

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