Article Text

Download PDFPDF
Familial Creutzfeldt–Jakob disease with E200K mutation presenting with neurosensorial hypoacusis

Statistics from Altmetric.com

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.

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.