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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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| Publicado no: | Brain Pathol |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Publishing Ltd
2006
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| Assuntos: | |
| Acesso em linha: | 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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