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Genetic prion disease: experience of a rapidly progressive dementia center in the United States and a review of the literature
Although prion diseases are generally thought to present as rapidly progressive dementias with survival of only a few months, the phenotypic spectrum for genetic prion diseases (gPrDs) is much broader. The majority have rapid decline with short survival but many present as slower progressive ataxic...
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| Yayımlandı: | Am J Med Genet B Neuropsychiatr Genet |
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| Asıl Yazarlar: | , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2017
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7207989/ https://ncbi.nlm.nih.gov/pubmed/27943639 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.32505 |
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