Neuromuscular Disorders
Volume 19, Issue 12 , Pages 845-848 , December 2009

Novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia and multisystem failure

  • S. Bohlega

      Affiliations

    • Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
    • Corresponding Author InformationCorresponding author. Address: Section of Neurology, Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Riyadh 11211, Saudi Arabia. Tel.: +966 1 464 7272x32819/32772.
    • ,
  • G. Van Goethem

      Affiliations

    • Department of Neurology, University Hospital Antwerp, Antwerpen, Belgium
    • Laboratory of Neurogenetics, Institute Born-Bunge, Antwerpen, Belgium
    • Department of Molecular Genetics, VIB, Antwerpen, Belgium
    • ,
  • A. Al Semari

      Affiliations

    • Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
    • ,
  • A. Löfgren

      Affiliations

    • Laboratory of Neurogenetics, Institute Born-Bunge, Antwerpen, Belgium
    • Department of Molecular Genetics, VIB, Antwerpen, Belgium
    • Department of Medical Genetics, University of Antwerp, Antwerpen, Belgium
    • ,
  • M. Al Hamed

      Affiliations

    • Research Center, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
    • ,
  • C. Van Broeckhoven

      Affiliations

    • Laboratory of Neurogenetics, Institute Born-Bunge, Antwerpen, Belgium
    • Department of Molecular Genetics, VIB, Antwerpen, Belgium
    • Department of Medical Genetics, University of Antwerp, Antwerpen, Belgium
    • ,
  • M. Kambouris

      Affiliations

    • Research Center, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia

Received 12 May 2009 ,Revised 29 August 2009 ,Accepted 2 October 2009.

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PII: S0960-8966(09)00653-1

doi: 10.1016/j.nmd.2009.10.002

Neuromuscular Disorders
Volume 19, Issue 12 , Pages 845-848 , December 2009

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