Variant CJD in an individual heterozygous for PRNP codon 129
- PMID: 20109837
- DOI: 10.1016/S0140-6736(09)61568-3
Variant CJD in an individual heterozygous for PRNP codon 129
Comment in
-
Variant or sporadic Creutzfeldt-Jakob disease?Lancet. 2010 Mar 13;375(9718):889; author reply 889-90. doi: 10.1016/S0140-6736(10)60378-9. Lancet. 2010. PMID: 20226976 No abstract available.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical