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Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy

Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e4bc73bf374343ccb8c9d259858dea64

Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy

About this item

Full title

Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy

Publisher

England: The Company of Biologists Ltd

Journal title

Disease models & mechanisms, 2015-03, Vol.8 (3), p.195-213

Language

English

Formats

Publication information

Publisher

England: The Company of Biologists Ltd

More information

Scope and Contents

Contents

Duchenne muscular dystrophy (DMD) is a progressive muscle-wasting disorder. It is caused by loss-of-function mutations in the dystrophin gene. Currently, there is no cure. A highly promising therapeutic strategy is to replace or repair the defective dystrophin gene by gene therapy. Numerous animal models of DMD have been developed over the last 30...

Alternative Titles

Full title

Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_e4bc73bf374343ccb8c9d259858dea64

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e4bc73bf374343ccb8c9d259858dea64

Other Identifiers

ISSN

1754-8403

E-ISSN

1754-8411

DOI

10.1242/dmm.018424

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