Neuromuscular Disorders
Volume 18, Issue 7 , Pages 579-582, July 2008

Phenotype of combined Duchenne and facioscapulohumeral muscular dystrophy☆☆☆

  • Lawrence Korngut

      Affiliations

    • Department of Clinical Neurosciences, Foothills Medical Centre, Heritage Medical Research Building, 182A-3330 Hospital Drive NW, Calgary, Alta., Canada T2N 4N1
    • Corresponding Author InformationCorresponding author. Tel.: +1 403 454 8599; fax: +1 403 283 8731.
    • ,
  • Victoria M. Siu

      Affiliations

    • Division of Pediatric Neurology, Childrens’ Hospital of Western Ontario, London, Canada
    • ,
  • Shannon L. Venance

      Affiliations

    • Department of Clinical Neurological Sciences, University Hospital, London, Canada
    • ,
  • Simon Levin

      Affiliations

    • Division of Pediatric Neurology, Childrens’ Hospital of Western Ontario, London, Canada
    • ,
  • Peter Ray

      Affiliations

    • Molecular Genetics, The Hospital for Sick Children, Toronto, Canada
    • ,
  • Richard J.L.F. Lemmers

      Affiliations

    • Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands
    • ,
  • Julia Keith

      Affiliations

    • Department of Pathology, University Hospital, London, Canada
    • ,
  • Craig Campbell

      Affiliations

    • Division of Pediatric Neurology, Childrens’ Hospital of Western Ontario, London, Canada

Received 9 August 2007; received in revised form 21 January 2008; accepted 14 March 2008.

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☆ Disclosures: None of the authors have competing interests.

☆☆ Note: Presented at the Canadian Congress of Neurological Sciences Annual Meeting, Montreal, Canada, June 2006.

PII: S0960-8966(08)00070-9

doi:10.1016/j.nmd.2008.03.011

Neuromuscular Disorders
Volume 18, Issue 7 , Pages 579-582, July 2008

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