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In vivo and in vitro investigations of heterozygous nebulin knock-out mice disclose a mild skeletal muscle phenotype. [electronic resource] by
- Gineste, C
- De Winter, J M
- Kohl, C
- Witt, C C
- Giannesini, B
- Brohm, K
- Le Fur, Y
- Gretz, N
- Vilmen, C
- Pecchi, E
- Jubeau, M
- Cozzone, P J
- Stienen, G J M
- Granzier, H
- Labeit, S
- Ottenheijm, C A C
- Bendahan, D
- Gondin, J
Producer: 20130903
In:
Neuromuscular disorders : NMD vol. 23
Availability: No items available.
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TPM3 deletions cause a hypercontractile congenital muscle stiffness phenotype. [electronic resource] by
- Donkervoort, S
- Papadaki, M
- de Winter, J M
- Neu, M B
- Kirschner, J
- Bolduc, V
- Yang, M L
- Gibbons, M A
- Hu, Y
- Dastgir, J
- Leach, M E
- Rutkowski, A
- Foley, A R
- Krüger, M
- Wartchow, E P
- McNamara, E
- Ong, R
- Nowak, K J
- Laing, N G
- Clarke, N F
- Ottenheijm, Cac
- Marston, S B
- Bönnemann, C G
Producer: 20160526
In:
Annals of neurology vol. 78
Availability: No items available.
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