Gene therapy via trans-splicing for LMNA-related congenital muscular dystrophy - Archive ouverte HAL
Poster De Conférence Année : 2018

Gene therapy via trans-splicing for LMNA-related congenital muscular dystrophy

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hal-03983935 , version 1 (11-02-2023)

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  • HAL Id : hal-03983935 , version 1

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F Azibani, A Brull, L Arandel, M Beuvin, I Nelson, et al.. Gene therapy via trans-splicing for LMNA-related congenital muscular dystrophy. Conference on Changing the Face of Modern Medicine - Stem Cell and Gene Therapy, Oct 2018, Lausanne, Switzerland. Hum. Gene Ther., 29 (12), pp.A138. P379, 2018. ⟨hal-03983935⟩
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