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Familial Creutzfeldt–Jakob disease with E200K mutation presenting with neurosensorial hypoacusis
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Footnotes
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Funding: This work was supported by the EU project Neuroprion.
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Competing interests: None declared.
Informed consent was obtained for publication of the patient’s details described in this report.
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Copyright information:
Copyright 2007 Journal of Neurology Neurosurgery and Psychiatry