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Category:Familial Creutzfeldt-Jakob Disease
Created 5 October 2007  +
CurationStatus uncurated  +
DefiningCitation N Engl J Med, 1998 Dec 31;339(27)  +
Definition A familial form exhibiting autosomal dominant inheritance has been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS (MeSH).
DefinitionSource MeSH +
Id birnlex_12688  +
Label Familial Creutzfeldt-Jakob Disease  +
Modification dateThis property is a special property in this wiki. 30 May 2009 03:29:16  +
ModifiedDate 30 May 2009  +
SuperCategory Creutzfeldt-Jakob Syndrome  +
Categories Creutzfeldt-Jakob Syndrome
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