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Encefalopatías espongiformes transmisibles: bases moleculares, diagnóstico y perspectivas terapéuticas

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Figure

FIGURA 1.-  Secuencias del cDNA y de los aminoácidos correspondientes en el gen PrP humano
FIGURA 3.-  Modelo para la formación de PrP SC  y estrategias para el diseño de drogas.
FIGURA 4.- Procedimiento experimental para la detección de formas patológicas de priones

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