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Letter
Familial Creutzfeldt–Jakob disease with E200K mutation presenting with neurosensorial hypoacusis

http://dx.doi.org/10.1136/jnnp.2006.095588

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    Footnotes

    • Funding: This work was supported by the EU project Neuroprion.

    • Competing interests: None declared.

      Informed consent was obtained for publication of the patient’s details described in this report.