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

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APA Style

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. 22(7), 1114–1114.

MLA Style

Petrie, K, et al. “An Atypical Mutation in the Activin a Receptor, Type 1 Gene (ACVR1) in a Severely Affected Fibrodysplasia Ossificans Progressiva Patient.” vol. 22, no. 7, 2007, pp. 1114–14.

Chicago Style

Petrie, K, J Pointon, R Smith, R Russell, P Wordsworth, and J Triffitt. 2007. “An Atypical Mutation in the Activin a Receptor, Type 1 Gene (ACVR1) in a Severely Affected Fibrodysplasia Ossificans Progressiva Patient.” 22 (7): 1114–14.
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+ Petrie, K More by this author

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+ Pointon, J More by this author

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+ Smith, R More by this author

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+ Russell, R More by this author

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+ Wordsworth, P More by this author

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Host title:: JOURNAL OF BONE AND MINERAL RESEARCH
Volume:: 22
Issue:: 7
Pages:: 1114-1114
Publication date:: 2007-07-01
ISSN:: 0884-0431

Pubs id:: pubs:108983
UUID:: uuid:f51373b1-89d5-4c2f-a99c-b37489b6a9d5
Local pid:: pubs:108983
Source identifiers:: 108983
Deposit date:: 2013-11-16
ARK identifier:: ark:/29072/ora_f51373b189d54c2fa99cb37489b6a9d5

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Copyright date:: 2007

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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