A case of V180I genetic mutation Creutzfeldt Jakob disease (CJD) with delusional misidentification as an initial symptom
Author:
Affiliation:
1. Department of Psychiatry, The Jikei University School of Medicine, Tokyo, Japan
2. Department of Psychiatry, Airanomori Hospital, Kagoshima, Japan
3. Department of Virology, The Jikei University School of Medicine, Tokyo, Japan
Funder
funding
Publisher
Informa UK Limited
Subject
Infectious Diseases,Cell Biology,Cellular and Molecular Neuroscience,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/19336896.2021.2017701
Reference30 articles.
1. Prospective 10-year surveillance of human prion diseases in Japan
2. Clinicopathological findings of a long-term survivor of V180I genetic Creutzfeldt-Jakob disease
3. Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene
4. The Neuropsychiatric Inventory: Assessing psychopathology in dementia patients
5. The Course of Psychopathologic Features in Mild to Moderate Alzheimer Disease
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4. Systematic Review of Clinical and Pathophysiological Features of Genetic Creutzfeldt–Jakob Disease Caused by a Val-to-Ile Mutation at Codon 180 in the Prion Protein Gene;International Journal of Molecular Sciences;2022-12-02
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