Abstract
Discovery of mutations of the PrnP gene without typical plaque formation and the characterization of two prion receptors led us to postulate a new class of prion-related disease: ‘loss of function’.
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Samaia, H., Brentani, R. Can loss-of-function prion-related diseases exist?. Mol Psychiatry 3, 196–197 (1998). https://doi.org/10.1038/sj.mp.4000378
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DOI: https://doi.org/10.1038/sj.mp.4000378
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