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Sporadic Jakob-Creutzfeldt disease, VV2 subtype, sagittal section of cerebellum with control cerebellum

Last updated on Friday, March 27 2009 by gliageek

Sporadic Jakob-Creutzfeldt disease, VV2 subtype, sagittal section of cerebellum with control cerebellum

In patients who are homozygous valine at codon 129 of the prion protein gene infected with type II prion demonstrate marked cerebellar degeneration responsible for severe ataxia seen in this variant

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