Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease.

Creutzfeldt-Jakob disease (CJD) belongs to a group of prion diseases that may be infectious, sporadic, or hereditary. The 200K point mutation in the PRNP gene is the most frequent cause of hereditary CJD, accounting for >70% of families with CJD worldwide. Prevalence of the 200K variant of famili...

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Autors principals: Lee, H S, Sambuughin, N, Cervenakova, L, Chapman, J, Pocchiari, M, Litvak, S, Qi, H Y, Budka, H, del Ser, T, Furukawa, H, Brown, P, Gajdusek, D C, Long, J C, Korczyn, A D, Goldfarb, L G
Format: Artigo
Idioma:Inglês
Publicat: 1999
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377830/
https://ncbi.nlm.nih.gov/pubmed/10090891
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