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
Poster De Conférence Année : 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

Domaines

Sciences du Vivant [q-bio]

Arnaud KLEIN  : Connectez-vous pour contacter le contributeur

https://hal.science/hal-04020115

Soumis le : mercredi 8 mars 2023-17:18:31

Dernière modification le : mardi 5 mars 2024-14:05:08

Fichier non déposé

Dates et versions

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

Identifiants

  • HAL Id : hal-04020115 , version 1

Citer

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⟩

Exporter

BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite

Collections

U974 USPC SORBONNE-UNIVERSITE SU-MEDECINE UP-SANTE U974-E4
20 Consultations
0 Téléchargements

Partager

More