Clinical features, lectin staining, and a novel GNE frameshift mutation in hereditary inclusion body myopathy

N C Voermans1, M Guillard, R Doedée

  • 1Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands. n.voermans@neuro.umcn.nl

Clinical Neuropathology
|February 24, 2010
PubMed

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