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Research Article

Dystrophin Gene Mutation Location and the Risk of Cognitive Impairment in Duchenne Muscular Dystrophy

  • Peter J. Taylor equal contributor,

    equal contributor Contributed equally to this work with: Peter J. Taylor, Grant A. Betts

    Affiliations: Molecular and Cytogenetics Unit, Department of Haematology and Genetics, Prince of Wales Hospital, Randwick, Sydney, New South Wales, Australia, Sydney Neuromuscular Centre, Sydney Children's Hospital, Randwick, Sydney, New South Wales, Australia

    X
  • Grant A. Betts equal contributor,

    equal contributor Contributed equally to this work with: Peter J. Taylor, Grant A. Betts

    Affiliation: Sydney Neuromuscular Centre, Sydney Children's Hospital, Randwick, Sydney, New South Wales, Australia

    X
  • Sarah Maroulis,

    Affiliation: Molecular and Cytogenetics Unit, Department of Haematology and Genetics, Prince of Wales Hospital, Randwick, Sydney, New South Wales, Australia

    X
  • Christian Gilissen,

    Affiliation: Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands

    X
  • Robyn L. Pedersen,

    Affiliation: Sydney Neuromuscular Centre, Sydney Children's Hospital, Randwick, Sydney, New South Wales, Australia

    X
  • David R. Mowat,

    Affiliations: Sydney Neuromuscular Centre, Sydney Children's Hospital, Randwick, Sydney, New South Wales, Australia, The School of Women's and Children's Health, University of New South Wales, Sydney, New South Wales, Australia

    X
  • Heather M. Johnston,

    Affiliation: Sydney Neuromuscular Centre, Sydney Children's Hospital, Randwick, Sydney, New South Wales, Australia

    X
  • Michael F. Buckley mail

    michael.buckley@sesiahs.health.nsw.gov.au

    Affiliations: Molecular and Cytogenetics Unit, Department of Haematology and Genetics, Prince of Wales Hospital, Randwick, Sydney, New South Wales, Australia, Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands

    X
  • Published: January 20, 2010
  • DOI: 10.1371/journal.pone.0008803

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