Cite
HARVARD Citation
Nagata, T. et al. (2022). A case of V180I genetic mutation Creutzfeldt Jakob disease (CJD) with delusional misidentification as an initial symptom. Prion. 16 (1), pp. 7-13. [Online].
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Nagata, T. et al. (2022). A case of V180I genetic mutation Creutzfeldt Jakob disease (CJD) with delusional misidentification as an initial symptom. Prion. 16 (1), pp. 7-13. [Online].