Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation. [electronic resource]

By: Contributor(s): Producer: 19960613Description: 758-61 p. digitalISSN:
  • 0028-3878
Subject(s): Online resources: In: Neurology vol. 46
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Publication Type: Case Reports; Journal Article

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