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No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease
BACKGROUND: A polymorphism at codon 129 of the prion protein gene (PRNP) is the only well-known genetic risk factor for Creutzfeldt-Jakob disease (CJD). However, there is increasing evidence that other loci outside the PRNP open reading frame might play a role in CJD aetiology as well. METHODS: We s...
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| Hlavní autoři: | , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2007
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2235832/ https://ncbi.nlm.nih.gov/pubmed/18072964 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-8-77 |
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