VP.42 Clinical characteristics, molecular genetics and long-term clinical outcomes in 43 patients with congenital myasthenia syndrome due to RAPSYN mutation
| Autor: | Ramdas, S., Munot, P., Cruz, P. Rodríguez, Alabaf, S., Robb, S., Jayawant, S., Beeson, D., Jungbluth, H., Palace, J. |
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| Zdroj: | In Neuromuscular Disorders October 2022 32 Supplement 1:S83-S83 |
| Databáze: | ScienceDirect |
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