G.P.5.02 LMNA is responsible for a recognisable form of congenital muscular dystrophy associated with selective axial muscle weakness and progressive course (L-CMD)
| Autor: | Quijano-Roy, S., Mbieleu, B., Bönnemann, C., Jeannet, P., Colomer, J., Clarke, N., Cuisset, J., Roper, H., De Meirleir, L., D’Amico, A., Ben Yaou, R., Barois, A., Demay, L., Romero, N., Sewry, C., Bertini, E., Ferreiro, A., Muntoni, F., Guicheney, P., Richard, P., Bonne, G., Estournet, B. |
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| Zdroj: | In Neuromuscular Disorders 2007 17(9):797-798 |
| Databáze: | ScienceDirect |
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