Creutzfeldt–Jakob disease in a Chinese patient with a novel seven extra-repeat insertion in PRNP

Familial transmissible spongiform encephalopathies comprise about 14% of all cases of transmissible spongiform encephalopathy in humans. We report on a patient with a definite diagnosis of familial Creutzfeldt–Jakob disease with an insertional mutation consisting of seven extra octapeptide repeats b...

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Detalhes bibliográficos
Main Authors: Wang, X F, Guo, Y J, Zhang, B Y, Zhao, W Q, Gao, J M, Wan, Y Z, Li, F, Han, J, Wang, D X, Dong, X P
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Publishing Group 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3029117/
https://ncbi.nlm.nih.gov/pubmed/21772923
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr.06.2009.2002
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