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The insomnia phenotype in genetic Creutzfeldt-Jakob disease based on the E200K mutation

Eva Feketeova1,2, Dominika Jarcuskova1,3, Alzbeta Janakova4

  • 1a Department of Neurology , P.J. Safarik University , Kosice , Slovakia.

Prion
|March 30, 2019
PubMed

Keywords:
E200KInsomniagenetic Creutzfeldt–Jakob diseasepolysomnographyprion diseases

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