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pubmed-article:18635614pubmed:abstractTextThe E200K mutation of the PRNP (prion protein) gene is the most common cause of familial Creutzfeldt-Jakob disease (fCJD), which has imaging and clinical features that are similar to the sporadic form. The purpose of this study was to conduct a controlled and blinded evaluation of the sensitivity and specificity of MR imaging in this unique population.lld:pubmed
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pubmed-article:18635614pubmed:articleTitleMR imaging of familial Creutzfeldt-Jakob disease: a blinded and controlled study.lld:pubmed
pubmed-article:18635614pubmed:affiliationDepartment of Radiology, Yale University School of Medicine, New Haven, CT 06520- 8043, USA. robert.fulbright@yale.edulld:pubmed
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