A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report
<p>Abstract</p> <p>Background</p> <p>Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare neurodegenerative disorder in humans included in the group of Transmissible Spongiform Encephalopathies or prion diseases. The vast majority of sCJD cases are molecularly classified...
| Main Authors: | , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2010-10-01
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| Series: | BMC Neurology |
| Online Access: | http://www.biomedcentral.com/1471-2377/10/99 |