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Mutations in dynamin 2 cause dominant centronuclear myopathy - Nature Genetics

  • ️Guicheney, Pascale
  • ️Sun Oct 16 2005

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Acknowledgements

We thank the affected individuals and their families for their participation in this study, J.P. Leroy and J.L. Mandel for continuous support, E. Ralston for comments and suggestions on the manuscript, A. Rouche for assistance with immunohistochemistry and C. Lacroix for providing a DNA sample. This work was supported by the Institut National de la Santé et de la Recherche Médicale, the Centre National de la Recherche Scientifique, the Hôpital Universitaire de Strasbourg, the Collège de France and the Association Française contre les Myopathies. H.L. is member of the German Muscular Dystrophy Network supported by the German Ministry of Education and Research. P.-Y.J. was a recipient of a fellowship from the Swiss Foundation for Research on Muscle Diseases. A.H.B. was supported by a grant from the US National Institutes of Health and the Joshua Frase Foundation. M.B. was the recipient of an Association Française contre les Myopathies fellowship.

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Authors and Affiliations

  1. INSERM U582, Institute of Myology, IFR14, Groupe Hospitalier Pitié-Salpêtrière, UPMC, 47 Boulevard de l'Hôpital, 75651, Paris Cedex 13, France

    Marc Bitoun, Svetlana Maugenre, Emmanuelle Lacène, Pascal Laforêt, Michel Fardeau, Bruno Eymard, Norma B Romero & Pascale Guicheney

  2. Department of Pediatrics, Neuropediatric Unit, CHUV, Lausanne, Switzerland

    Pierre-Yves Jeannet

  3. Department of Neurology, CHU Haut-Lévêque, Bordeaux, France

    Xavier Ferrer

  4. Laboratory of Neuropathology, Born-Bunge Institute, Antwerp, Belgium

    Jean-Jacques Martin

  5. Department of Molecular Pathology, I.G.B.M.C., CNRS/INSERM/ULP/Collège de France, Illkirch, France

    Jocelyn Laporte

  6. Department of Neurology, Friedrich Baur Institute, Ludwig Maximilians University, Munich, Germany

    Hanns Lochmüller

  7. Genetics Division, Children's Hospital Boston, Harvard Medical School, Boston, USA

    Alan H Beggs

Authors

  1. Marc Bitoun

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  2. Svetlana Maugenre

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  3. Pierre-Yves Jeannet

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  4. Emmanuelle Lacène

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  5. Xavier Ferrer

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  6. Pascal Laforêt

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  7. Jean-Jacques Martin

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  8. Jocelyn Laporte

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  9. Hanns Lochmüller

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  10. Alan H Beggs

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  11. Michel Fardeau

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  12. Bruno Eymard

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  13. Norma B Romero

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  14. Pascale Guicheney

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Corresponding author

Correspondence to Pascale Guicheney.

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The authors declare no competing financial interests.

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Bitoun, M., Maugenre, S., Jeannet, PY. et al. Mutations in dynamin 2 cause dominant centronuclear myopathy. Nat Genet 37, 1207–1209 (2005). https://doi.org/10.1038/ng1657

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  • Received: 22 March 2005

  • Accepted: 23 August 2005

  • Published: 16 October 2005

  • Issue Date: 01 November 2005

  • DOI: https://doi.org/10.1038/ng1657