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The insomnia phenotype in genetic Creutzfeldt–Jakob disease based on the E200K mutation
The aim of the presented study was to reveal the frequency of insomnia spells in E200K genetic Creutzfeldt–Jakob disease (gCJD) patients. Clinical records of 22 subjects diagnosed with E200K gCJD were retrospectively reviewed. The patients w/wo insomnia (n = 4, 18%/n = 18, 82%) did not differ in age...
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| Publicado no: | Prion |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7000144/ https://ncbi.nlm.nih.gov/pubmed/30922182 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2019.1590938 |
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