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Neuropathological findings from a human post mortem case of distal hereditary motor neuropathy (dHMN) due to p.Ser135Phe HSPB1 mutation and transgenic mice with mutant or wild-type HSP27 overexpression
Phadke, R., Rossor, A., Benoy, V., Kalmar, B., King, R., Greensmith, L., Bosch, L., Reilly, M., Houlden, H.Volume:
25
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2015.06.348
Date:
October, 2015
File:
PDF, 204 KB
english, 2015