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55921.
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55922.
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55923.
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Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia. [electronic resource] by
- Peyer, Anne-Kathrin
- Kinter, Jochen
- Hench, Jürgen
- Frank, Stephan
- Fuhr, Peter
- Thomann, Sandra
- Fischmann, Arne
- Kneifel, Stefan
- Camaño, Pilar
- López de Munain, Adolfo
- Sinnreich, Michael
- Renaud, Susanne
Producer: 20130905
In:
Neuromuscular disorders : NMD vol. 23
Availability: No items available.
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