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Familial clustering of the ataxic form of Creutzfeldt-Jakob disease with Hirano bodies.

A family cluster of the ataxic form of Creutzfeldt-Jakob disease with one probable and two autopsy proven cases that occurred in a single generation between 1974 and 1982 is reported. The clinical characteristics of the cases are closely similar to those of kuru patients, with a fair correlation bet...

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Detaylı Bibliyografya
Asıl Yazarlar: Cartier, L, Gálvez, S, Gajdusek, D C
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1985
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1028256/
https://ncbi.nlm.nih.gov/pubmed/2984334
Etiketler: Etiketle
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