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Research Article

A Mutation in the Mitochondrial Fission Gene Dnm1l Leads to Cardiomyopathy

  • Houman Ashrafian,

    Affiliation: Department of Cardiovascular Medicine and Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • Louise Docherty,

    Affiliation: Mammalian Genetics of Disease Unit, School of Medicine, University of Sheffield, Sheffield, United Kingdom

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  • Vincenzo Leo,

    Affiliation: Leeds Institute of Molecular Medicine, Wellcome Trust Brenner Building, St. James's University Hospital, Leeds, United Kingdom

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  • Christopher Towlson,

    Affiliation: Mammalian Genetics of Disease Unit, School of Medicine, University of Sheffield, Sheffield, United Kingdom

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  • Monica Neilan,

    Affiliation: Mammalian Genetics of Disease Unit, School of Medicine, University of Sheffield, Sheffield, United Kingdom

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  • Violetta Steeples,

    Affiliation: Department of Cardiovascular Medicine and Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • Craig A. Lygate,

    Affiliation: Department of Cardiovascular Medicine and Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • Tertius Hough,

    Affiliation: Leeds Institute of Molecular Medicine, Wellcome Trust Brenner Building, St. James's University Hospital, Leeds, United Kingdom

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  • Stuart Townsend,

    Affiliation: Leeds Institute of Molecular Medicine, Wellcome Trust Brenner Building, St. James's University Hospital, Leeds, United Kingdom

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  • Debbie Williams,

    Affiliation: Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council, Harwell, United Kingdom

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  • Sara Wells,

    Affiliation: Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council, Harwell, United Kingdom

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  • Dominic Norris,

    Affiliation: Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council, Harwell, United Kingdom

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  • Sarah Glyn-Jones,

    Affiliation: Department of Biochemistry, University of Cambridge, Cambridge, United Kingdom

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  • John Land,

    Affiliation: Neurometabolic Unit, National Hospital, London, United Kingdom

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  • Ivana Barbaric,

    Affiliation: Department of Biomedical Science, University of Sheffield, Sheffield, United Kingdom

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  • Zuzanne Lalanne,

    Affiliation: Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council, Harwell, United Kingdom

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  • Paul Denny,

    Affiliation: Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council, Harwell, United Kingdom

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  • Dorota Szumska,

    Affiliation: Department of Cardiovascular Medicine and Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • Shoumo Bhattacharya,

    Affiliation: Department of Cardiovascular Medicine and Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • Julian L. Griffin,

    Affiliation: Department of Biochemistry, University of Cambridge, Cambridge, United Kingdom

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  • Iain Hargreaves,

    Affiliation: Neurometabolic Unit, National Hospital, London, United Kingdom

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  • Narcis Fernandez-Fuentes,

    Affiliation: Leeds Institute of Molecular Medicine, Wellcome Trust Brenner Building, St. James's University Hospital, Leeds, United Kingdom

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  • Michael Cheeseman,

    Affiliation: Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council, Harwell, United Kingdom

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  • Hugh Watkins,

    Affiliation: Department of Cardiovascular Medicine and Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • T. Neil Dear mail

    t.n.dear@leeds.ac.uk

    Affiliations: Mammalian Genetics of Disease Unit, School of Medicine, University of Sheffield, Sheffield, United Kingdom, Leeds Institute of Molecular Medicine, Wellcome Trust Brenner Building, St. James's University Hospital, Leeds, United Kingdom, Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council, Harwell, United Kingdom

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  • Published: June 24, 2010
  • DOI: 10.1371/journal.pgen.1001000

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