Petrie, K., Pointon, J., Smith, R., Russell, R., Wordsworth, P., & Triffitt, J. (2007). An atypical mutation in the activin a receptor, type 1 gene (ACVR1) in a severely affected Fibrodysplasia Ossificans Progressiva patient.
Lua i Stíl Chicago (17ú heag.)Petrie, K., J. Pointon, R. Smith, R. Russell, P. Wordsworth, agus J. Triffitt. An Atypical Mutation in the Activin a Receptor, Type 1 Gene (ACVR1) in a Severely Affected Fibrodysplasia Ossificans Progressiva Patient. 2007.
Lua MLA (9ú heag.)Petrie, K., et al. An Atypical Mutation in the Activin a Receptor, Type 1 Gene (ACVR1) in a Severely Affected Fibrodysplasia Ossificans Progressiva Patient. 2007.
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