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.
Zdroj: In Neuromuscular Disorders October 2021 31 Supplement 1:S70-S70
Databáze: ScienceDirect