La maladie de Creutzfeldt-Jakob génétique due à la mutation E200K : une maladie aux multiples facettes
Autor: Hasier Eraña Un estudio internacional recientemente publicado en la revista científica Acta Neuropathologica (puede acceder al artículo original, en inglés, aquí) ha analizado en profundidad la enfermedad de Creutzfeldt-Jakob genética (ECJ genética) causada por la mutación E200K, la forma hereditaria más frecuente de las enfermedades priónicas humanas. Se trata del mayor estudio realizado hasta […]
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Overexpression of bank vole PrP(I109) in mice induces a spontaneous atypical prion disease with sex-dependent onset, early NfL elevation, and universal prion strain permissiveness
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