CONGENITAL MUSCULAR DYSTROPHIES: EP.68 Therapeutic effect of linker protein-mediated gene therapy in a mouse model for LAMA2-related muscular dystrophy
Autor: | Reinhard, J., Lin, S., Rüegg, M. |
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Zdroj: | In Neuromuscular Disorders October 2021 31 Supplement 1:S70-S70 |
Databáze: | ScienceDirect |
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