Research ArticleMuscular Dystrophy

A Human-Specific Deletion in Mouse Cmah Increases Disease Severity in the mdx Model of Duchenne Muscular Dystrophy

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Science Translational Medicine  28 Jul 2010:
Vol. 2, Issue 42, pp. 42ra54
DOI: 10.1126/scitranslmed.3000692

Article Information

vol. 2 no. 42 42ra54

PubMed: 
Print ISSN: 
Online ISSN: 
History: 
  • Received for publication December 1, 2009
  • Accepted for publication July 9, 2010
  • .

Author Information

  1. Kumaran Chandrasekharan1,
  2. Jung Hae Yoon1,
  3. Ying Xu2,
  4. Sarah deVries1,
  5. Marybeth Camboni1,
  6. Paulus M. L. Janssen2,
  7. Ajit Varki3 and
  8. Paul T. Martin1,2,4,*
  1. 1Center for Gene Therapy, Research Institute at Nationwide Children’s Hospital, 700 Children’s Drive, Columbus, OH 43205, USA.
  2. 2Department of Physiology and Cell Biology, Ohio State University College of Medicine, Columbus, OH 43210, USA.
  3. 3Departments of Medicine and Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
  4. 4Department of Pediatrics, Ohio State University College of Medicine, Columbus, OH 43205, USA.
  1. *To whom correspondence should be addressed. E-mail: paul.martin{at}nationwidechildrens.org

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