Paper Tools Add to my Library Share How would you like to share? Facebook Twitter LinkedIn Back to the Top
Nagata T, Shinagawa S, Kobayashi N, Kondo K, Shigeta M. A case of V180I genetic mutation Creutzfeldt Jakob disease (CJD) with delusional misidentification as an initial symptom. Prion. 2022 Dec;16(1):7-13. PubMed. Recommends Please login to recommend the paper. Comments No Available Comments Make a Comment To make a comment you must login or register.
Comments
No Available Comments
Make a Comment
To make a comment you must login or register.