The First Sporadic Creutzfeldt–Jakob Disease Case with a Rare Molecular Subtype VV1 and 1-Octapeptide Repeat Deletion in PRNP |
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| Authors: | Auš rinė Areš kevič iū tė ,Eva Lø bner Lund,Sabina Capellari,Piero Parchi,Christian Tersbø l Pinkowsky |
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| Affiliation: | 1.Department of Pathology, Danish Reference Center for Prion Diseases, Copenhagen University Hospital, 2100 Copenhagen, Denmark; (A.A.); (E.L.L.);2.IRCCS Istituto delle Scienze Neurologiche di Bologna, Ospedale Bellaria, 40123 Bologna, Italy; (S.C.); (P.P.);3.Department of Experimental Diagnostic and Specialty Medicine (DIMES), University of Bologna, 40126 Bologna, Italy;4.Department of Spinal Cord Injuries, Copenhagen University Hospital, 3100 Hornbæk, Denmark |
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| Abstract: | ![]()
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| Keywords: | Creutzfeldt– Jakob disease, 1-OPRD, VV1, sporadic prion disease, prions, 58-year-old female patient, prion protein gene, deletion polymorphism |
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