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

  * E-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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