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Rare variants in MME, encoding metalloprotease neprilysin, are linked to late-onset autosomal-dominant axonal polyneuropathies. by Auer-Grumbach, M, Toegel, S, Schabhüttl, M, Weinmann, D, Chiari, C, Bennett, D, Beetz, C, Klein, D, Andersen, P, Böhme, I, Fink-Puches, R, Gonzalez, M, Harms, M, Motley, W, Reilly, M, Renner, W, Rudnik-Schöneborn, S, Schlotter-Weigel, B, Themistocleous, A, Weishaupt, J, Ludolph, A, Wieland, T, Tao, F, Abreu, L, Windhager, R, Zitzelsberger, M, Strom, T, Walther, T, Scherer, S, Züchner, S, Martini, R, Senderek, J
Published 2016Journal article