Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein Gene.
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| Description | scientific article |
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author: Gabriella Marcon Antonio Indaco Giuseppe Di Fede Giorgio Giaccone Veronica Redaelli Pietro Zerbi Fabrizio Tagliavini Silvia Suardi Paolo Fociani |
| Publication date | November 27, 2013 |
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