Identification of the gene causing dilated cardiomyopathy with ataxia syndrome (DCMA), a Novel Barth syndrome-like condition in the Hutterite population

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dc.contributor.advisorBridge, Peter
dc.contributor.advisorBernier, Francois P.
dc.contributor.authorDavey, Krista Michelle
dc.date.accessioned2017-12-18T21:16:26Z
dc.date.available2017-12-18T21:16:26Z
dc.date.issued2006
dc.descriptionBibliography: p. 187-201en
dc.descriptionSome pages are in colour.en
dc.format.extentxiv, 259 leaves : ill. ; 30 cm.en
dc.identifier.citationDavey, K. M. (2006). Identification of the gene causing dilated cardiomyopathy with ataxia syndrome (DCMA), a Novel Barth syndrome-like condition in the Hutterite population (Master's thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca. doi:10.11575/PRISM/836en_US
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/836
dc.identifier.urihttp://hdl.handle.net/1880/101837
dc.language.isoeng
dc.publisher.institutionUniversity of Calgaryen
dc.publisher.placeCalgaryen
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.
dc.titleIdentification of the gene causing dilated cardiomyopathy with ataxia syndrome (DCMA), a Novel Barth syndrome-like condition in the Hutterite population
dc.typemaster thesis
thesis.degree.disciplineMedical Science
thesis.degree.grantorUniversity of Calgary
thesis.degree.nameMaster of Science (MSc)
ucalgary.thesis.accessionTheses Collection 58.002:Box 1638 520492155
ucalgary.thesis.notesUARCen
ucalgary.thesis.uarcreleaseyen
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