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Journal article

Therapeutic approaches to muscular dystrophy.

Abstract:: Muscular dystrophies are a heterogeneous group of genetic disorders characterized by muscle weakness and wasting. Duchenne muscular dystrophy (DMD) is the most common and severe form of muscular dystrophy, and although the molecular mechanisms of the disease have been extensively investigated since the discovery of the gene in 1986, there is currently no effective treatment. However, new gene-based therapies have recently emerged with particular noted advances in using conventional gene repla...
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Publication status:: Published

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APA Style

Goyenvalle, A., Seto, J., Davies, K., & Chamberlain, J. (2011). Therapeutic approaches to muscular dystrophy. Human Molecular Genetics, 20(R1), R69–R78.

MLA Style

Goyenvalle, A., et al. “Therapeutic Approaches to Muscular Dystrophy.” Human Molecular Genetics, vol. 20, no. R1, 2011, pp. R69–R78.

Chicago Style

Goyenvalle, A, J Seto, K Davies, and J Chamberlain. 2011. “Therapeutic Approaches to Muscular Dystrophy.” Human Molecular Genetics 20 (R1): R69–R78.
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Publisher copy:: 10.1093/hmg/ddr105

Authors

+ Goyenvalle, A More by this author

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Author

+ Seto, J More by this author

Role:

Author

+ Davies, K More by this author

Institution:

University of Oxford

Division:

MSD

Department:

Physiology Anatomy & Genetics

Role:

Author

+ Chamberlain, J More by this author

Role:

Author

Bibliographic Details

Journal:: Human molecular genetics
Volume:: 20
Issue:: R1
Pages:: R69-R78
Publication date:: 2011-04-01
DOI:: 10.1093/hmg/ddr105
EISSN:: 1460-2083
ISSN:: 0964-6906

Item Description

Language:: English
Keywords:: Humans

Muscular Dystrophies

Dystrophin

Exons

Genetic Therapy
Pubs id:: pubs:127193
UUID:: uuid:0b20898a-8651-437b-ad4c-67b0752fdad0
Local pid:: pubs:127193
Source identifiers:: 127193
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2011

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

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