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Case Reports in Medicine
Volume 2009, Article ID 183125, 3 pages
http://dx.doi.org/10.1155/2009/183125
Case Report

A Case of Dilated Cardiomyopathy Associated with 3-Hydroxy-3-Methylglutaryl-Coenzyme A (HMG CoA) Lyase Deficiency

1Department of Medicine, University of Alberta Hospital, University of Alberta, Edmonton, AB, Canada T6G 2B7
2Department of Medical Genetics, University of Alberta/Stollery Children's Hospital, University of Alberta, Edmonton, AB, Canada T6G 2B7
3Department of Pediatrics, Alberta Children's Hospital, University of Calgary, Calgary, AB, Canada T2M 0H5

Received 25 June 2009; Accepted 29 September 2009

Academic Editor: André Meégarbaneé

Copyright © 2009 Alexander A. C. Leung et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citations to this Article [10 citations]

The following is the list of published articles that have cited the current article.

  • Beatriz Puisac, Maria Arnedo, Cesar H. Casale, Maria Pilar Ribate, Tomas Castiella, Feliciano J. Ramos, Antonia Ribes, Celia Perez-Cerda, Nuria Casals, Fausto G. Hegardt, and Juan Pie, “Differential HMG-CoA lyase expression in human tissues provides clues about 3-hydroxy-3-methylglutaric aciduria,” Journal Of Inherited Metabolic Disease, vol. 33, no. 4, pp. 405–410, 2010. View at Publisher · View at Google Scholar
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