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pubmed-article:20049325pubmed:abstractTextPrion diseases are a family of rare, progressive, neurodegenerative disorders that affect humans and animals. The most common form of human prion disease, Creutzfeldt-Jakob disease (CJD), occurs worldwide. Variant CJD (vCJD), a recently emerged human prion disease, is a zoonotic foodborne disorder that occurs almost exclusively in countries with outbreaks of bovine spongiform encephalopathy. This study describes the occurrence and epidemiology of CJD and vCJD in the United States.lld:pubmed
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pubmed-article:20049325pubmed:year2010lld:pubmed
pubmed-article:20049325pubmed:articleTitleHuman prion diseases in the United States.lld:pubmed
pubmed-article:20049325pubmed:affiliationDivision of Viral and Rickettsial Diseases, National Center for Zoonotic, Vector-borne and Enteric Diseases, Centers for Disease Control and Prevention (CDC), U.S. Department of Health and Human Services (USDHHS), Atlanta, Georgia, United States of America. rholman@cdc.govlld:pubmed
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