The BALB/c.mdx62 mouse exhibits a dystrophic muscle pathology and is a model of Duchenne muscular dy...
The BALB/c.mdx62 mouse exhibits a dystrophic muscle pathology and is a model of Duchenne muscular dystrophy
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Author / Creator
Publisher
The Company of Biologists Ltd
Journal title
Language
English
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Publication information
Publisher
The Company of Biologists Ltd
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Scope and Contents
Contents
Duchenne muscular dystrophy (DMD) is a devastating monogenic skeletal muscle-wasting disorder. Although many pharmacological and genetic interventions have been reported in preclinical studies, few have progressed to clinical trials with meaningful benefit. Identifying therapeutic potential can be limited by availability of suitable preclinical mou...
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Full title
The BALB/c.mdx62 mouse exhibits a dystrophic muscle pathology and is a model of Duchenne muscular dystrophy
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Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_0b8d5a9dc15b471b9c11baee9e4ca30c
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_0b8d5a9dc15b471b9c11baee9e4ca30c
Other Identifiers
ISSN
1754-8403
E-ISSN
1754-8411
DOI
10.1242/dmm.050502
