In vivo genome editing mediates resection of the CTG repeat expansion and decreases pathological signs in a mouse model of myotonic dystrophy type 1 - Archive ouverte HAL Access content directly
Poster Communications Year : 2019

In vivo genome editing mediates resection of the CTG repeat expansion and decreases pathological signs in a mouse model of myotonic dystrophy type 1

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hal-04020115 , version 1 (08-03-2023)

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  • HAL Id : hal-04020115 , version 1

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Mirella Lo Scrutado, Karine Poulard, C. Sourd, Stéphanie Tomé, Arnaud F Klein, et al.. In vivo genome editing mediates resection of the CTG repeat expansion and decreases pathological signs in a mouse model of myotonic dystrophy type 1. 6th International Congress of Myology, Mar 2019, Bordeaux, France. ⟨hal-04020115⟩
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