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Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/7152
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dc.contributor.authorBassett, D Ien_UK
dc.contributor.authorCurrie, Peter Den_UK
dc.date.accessioned2017-01-13T23:18:00Z-
dc.date.available2017-01-13T23:18:00Zen_UK
dc.date.issued2003-10-15en_UK
dc.identifier.urihttp://hdl.handle.net/1893/7152-
dc.description.abstractThe muscular dystrophies and congenital myopathies are inherited diseases of the skeletal muscle, which lead to a loss of muscle function and are often fatal. While many of the loci involved are already known, these conditions remain incurable, and genetic models are being developed in an effort to understand the pathological mechanisms involved. Recently several papers have shown that the zebrafish, which is now widely used in developmental genetic studies, will provide a useful addition to our toolkit in this regard. Here we describe these studies, including a zebrafish model of what is potentially the novel pathological mechanism of muscle attachment failure in Duchenne and other muscular dystrophies.en_UK
dc.language.isoenen_UK
dc.publisherOxford University Pressen_UK
dc.relationBassett DI & Currie PD (2003) The zebrafish as a model for muscular dystrophy and congenital myopathy. Human Molecular Genetics, 12 (Supplement 2), pp. R265-R270. https://doi.org/10.1093/hmg/ddg279en_UK
dc.rightsThe publisher does not allow this work to be made publicly available in this Repository. Please use the Request a Copy feature at the foot of the Repository record to request a copy directly from the author. You can only request a copy if you wish to use this work for your own research or private study.en_UK
dc.rights.urihttp://www.rioxx.net/licenses/under-embargo-all-rights-reserveden_UK
dc.titleThe zebrafish as a model for muscular dystrophy and congenital myopathyen_UK
dc.typeJournal Articleen_UK
dc.rights.embargodate2999-12-16en_UK
dc.rights.embargoreason[Bassett 2003.pdf] The publisher does not allow this work to be made publicly available in this Repository therefore there is an embargo on the full text of the work.en_UK
dc.identifier.doi10.1093/hmg/ddg279en_UK
dc.citation.jtitleHuman Molecular Geneticsen_UK
dc.citation.issn1460-2083en_UK
dc.citation.issn0964-6906en_UK
dc.citation.volume12en_UK
dc.citation.issueSupplement 2en_UK
dc.citation.spageR265en_UK
dc.citation.epageR270en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.author.emaild.i.bassett@stir.ac.uken_UK
dc.contributor.affiliationMachrihanishen_UK
dc.contributor.affiliationVictor Chang Cardiac Research Instituteen_UK
dc.identifier.isiWOS:000185896800018en_UK
dc.identifier.wtid791089en_UK
dc.contributor.orcid0000-0002-7529-0829en_UK
dc.date.accepted2003-08-08en_UK
dcterms.dateAccepted2003-08-08en_UK
dc.date.filedepositdate2012-08-01en_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorBassett, D I|0000-0002-7529-0829en_UK
local.rioxx.authorCurrie, Peter D|en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate2999-12-16en_UK
local.rioxx.licencehttp://www.rioxx.net/licenses/under-embargo-all-rights-reserved||en_UK
local.rioxx.filenameBassett 2003.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source0964-6906en_UK
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