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

• Peter J. Taylor ,

  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

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• Grant A. Betts ,

  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

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• Sarah Maroulis,

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

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• Christian Gilissen,

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

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• Robyn L. Pedersen,

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

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• 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

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• Heather M. Johnston,

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

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• Michael F. Buckley

  * E-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

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