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Functional investigation of beta-tropomyosin mutations that cause congenital skeletal myopathies

Publication status:: Published

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APA Style

Piers, A., Robinson, P., & Redwood, C. (2011). Functional investigation of beta-tropomyosin mutations that cause congenital skeletal myopathies. NEUROMUSCULAR DISORDERS, 21, S25–S26.

MLA Style

Piers, A., et al. “Functional Investigation of Beta-Tropomyosin Mutations That Cause Congenital Skeletal Myopathies.” NEUROMUSCULAR DISORDERS, vol. 21, 2011, pp. S25–S26.

Chicago Style

Piers, A, P Robinson, and C Redwood. 2011. “Functional Investigation of Beta-Tropomyosin Mutations That Cause Congenital Skeletal Myopathies.” In NEUROMUSCULAR DISORDERS, 21:S25–S26.
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Authors

+ Piers, A More by this author

Role:: Author

+ Robinson, P More by this author

Role:: Author

+ Redwood, C More by this author

Role:: Author

Host title:: NEUROMUSCULAR DISORDERS
Volume:: 21
Pages:: S25-S26
Publication date:: 2011-03-01
ISSN:: 0960-8966

Pubs id:: pubs:138880
UUID:: uuid:4a47acd2-fe49-46cd-87d2-399369976a20
Local pid:: pubs:138880
Source identifiers:: 138880
Deposit date:: 2012-12-19

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Copyright date:: 2011

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

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