{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,3,28]],"date-time":"2024-03-28T19:14:46Z","timestamp":1711653286206},"reference-count":19,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2001,7,3]],"date-time":"2001-07-03T00:00:00Z","timestamp":994118400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Annals of Neurology"],"published-print":{"date-parts":[[2001,8]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>A case of sporadic Creutzfeldt\u2010Jakob disease (sCJD) is described in a young Dutch protein prion gene <jats:italic>(PRNP)<\/jats:italic> codon 129 valine homozygote. Certain clinical and molecular features of this case overlap those of variant CJD. 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