An atypical mutation in the activin a receptor, type 1 gene (ACVR1) in a severely affected Fibrodysplasia Ossificans Progressiva patient
Prif Awduron: | Petrie, K, Pointon, J, Smith, R, Russell, R, Wordsworth, P, Triffitt, J |
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Fformat: | Conference item |
Cyhoeddwyd: |
2007
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Eitemau Tebyg
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Identification of a novel mutation in activin receptor type 1 (ACVR1) in a fibrodysplasia ossificans progressiva (FOP) patient
gan: Petrie, K, et al.
Cyhoeddwyd: (2007) -
Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
gan: Petrie, K, et al.
Cyhoeddwyd: (2009) -
Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
gan: Petrie, K, et al.
Cyhoeddwyd: (2009) -
ACVR1 mutation and Fibrodysplasia Ossificans Progressiva in Chinese children
gan: Ng Bobby KW, et al.
Cyhoeddwyd: (2011-09-01) -
Mutation Detection in Activin A Receptor, Type I (ACVR1) Gene in Fibrodysplasia Ossificans Progressiva in An Iranian Family
gan: Ziba Morovvati, et al.
Cyhoeddwyd: (2014-03-01)