Rare variants in MME, encoding metalloprotease neprilysin, are linked to late-onset autosomal-dominant axonal polyneuropathies
by Auer-Grumbach, Michaela (Author)
, Toegel, Stefan (Author)
, Schabhüttl, Maria (Author)
, Weinmann, Daniela (Author)
, Chiari, Catharina (Author)
, Bennett, David L. H. (Author)
, Beetz, Christian (Author)
, Klein, Dennis (Author)
, Andersen, Peter M. (Author)
, Böhme, Ilka (Author)
, Fink-Puches, Regina (Author)
, Gonzalez, Michael (Author)
, Harms, Matthew B. (Author)
, Motley, William (Author)
, Reilly, Mary M. (Author)
, Renner, Wilfried (Author)
, Rudnik-Schöneborn, Sabine (Author)
, Schlotter-Weigel, Beate (Author)
, Themistocleous, Andreas C. (Author)
, Weishaupt, Jochen H. (Author)
, Ludolph, Albert C. (Author)
, Wieland, Thomas (Author)
, Tao, Feifei (Author)
, Abreu, Lisa (Author)
, Windhager, Reinhard (Author)
, Zitzelsberger, Manuela (Author)
, Strom, Tim M. (Author)
, Walther, Thomas (Author)
, Scherer, Steven S. (Author)
, Züchner, Stephan (Author)
, Martini, Rudolf (Author)
, Senderek, Jan (Author)
,
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