Mutations in EIF4G1 are not a common cause of Parkinson's disease

Authors

  • A. Siitonen,

    Corresponding author
    1. Department of Clinical Medicine, Neurology, University of Oulu, Oulu, Finland
    2. Department of Neurology, Oulu University Hospital, Oulu, Finland
    • Correspondence: A. B. Siitonen, MSc, BM, Department of Neurology, University of Oulu, P.O. Box 5000, FIN-90014 Oulu, Finland (tel.: +358-8-315 4526; fax: +358-8-315 4544; e-mail: Ari.Siitonen@iki.fi).

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  • E. Majounie,

    1. Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA
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  • M. Federoff,

    1. Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA
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  • J. Ding,

    1. Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA
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  • K. Majamaa,

    1. Department of Clinical Medicine, Neurology, University of Oulu, Oulu, Finland
    2. Department of Neurology, Oulu University Hospital, Oulu, Finland
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  • A. B. Singleton

    1. Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA
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No abstract is available for this article.

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