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Conclusions of the Symposium
On the basis of twenty‐one kindreds and three cases from uninformative families, the Symposium has confirmed that fatal familial insomnia (FFI) is genotypically and phenotypically distinct and, likely, the third most common inherited prion disease. The genotype, characterized by the D178N mutation o...
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| Yayımlandı: | Brain Pathol |
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| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Blackwell Publishing Ltd
2006
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8098585/ https://ncbi.nlm.nih.gov/pubmed/9669714 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1750-3639.1998.tb00185.x |
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