Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia
Peyer, Anne-Kathrin, Kinter, Jochen, Hench, Jürgen, Frank, Stephan, Fuhr, Peter, Thomann, Sandra, Fischmann, Arne, Kneifel, Stefan, Camaño, Pilar, Munain, Adolfo López de, Sinnreich, Michael, Renaud,Volume:
23
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2012.09.009
Date:
February, 2013
File:
PDF, 823 KB
english, 2013