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Grasbon-Frodl, E; Lorenz, H; Mann, U; Nitsch, R M; Windl, O; Kretzschmar, H A (2004). Loss of glycosylation associated with the T183A mutation in human prion disease. Acta Neuropathologica, 108(6):476-484.

This list was generated on Sun Nov 19 19:13:57 2017 CET.