A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report

BACKGROUND: Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare neurodegenerative disorder in humans included in the group of Transmissible Spongiform Encephalopathies or prion diseases. The vast majority of sCJD cases are molecularly classified according to the abnormal prion protein (PrP(Sc)) conf...

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Detalles Bibliográficos
Autores principales: Rodríguez-Martínez, Ana B, Garrido, Joseba M, Zarranz, Juan J, Arteagoitia, Jose M, de Pancorbo, Marian M, Atarés, Begoña, Bilbao, Miren J, Ferrer, Isidro, Juste, Ramón A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2987858/
https://www.ncbi.nlm.nih.gov/pubmed/20973975
http://dx.doi.org/10.1186/1471-2377-10-99

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2987858/
https://www.ncbi.nlm.nih.gov/pubmed/20973975
http://dx.doi.org/10.1186/1471-2377-10-99

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