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Ullrich myopathy phenotype with secondary ColVI defect identified by confocal imaging and electron microscopy analysis. [electronic resource] by
- Petrini, Stefania
- D'Amico, Adele
- Sale, Patrizio
- Lucarini, Laura
- Sabatelli, Patrizia
- Tessa, Alessandra
- Giusti, Betti
- Verardo, Margherita
- Carrozzo, Rosalba
- Mattioli, Elisabetta
- Scarpelli, Marina
- Chu, Mon-Li
- Pepe, Guglielmina
- Russo, Matteo Antonio
- Bertini, Enrico
Producer: 20071009
In:
Neuromuscular disorders : NMD vol. 17
Availability: No items available.
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6640.
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