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Journal article

Auer-Grumbach, M.; Bennett, D. L. H.; Andersen, P.; Harms, M. B.; Reilly, M. M.; Weishaupt, J.; Strom, T. M.; Walther, T.; Scherer, S. S.; Zuchner, S.; Martini, R.; Senderek, J. (2016): Rare coding variants in the mme gene, encoding the metalloprotease neprilysin, are linked to late-onset axonal neuropathies. In: Journal of the Peripheral Nervous System, Vol. 21, No. 3: p. 235

Schüle, R.; Kremer, B.P.H.; Kassubek, J.; Auer-Grumbach, M.; Kostic, V.; Klopstock, Thomas; Klimpe, S.; Otto, S.; Boesch, S.; van de Warrenburg, B.P.; Schöls, L. (2008): SPG10 is a rare cause of spastic paraplegia in European families. In: Journal of Neurology, Neurosurgery & Psychiatry, Vol. 79, No. 5: pp. 584-587 [PDF, 336kB]

This list was generated on Thu Apr 25 05:21:06 2019 CEST.