AAV-mediated cardiac gene transfer of wild-type desmin in mouse models for recessive desminopathies

por Ruppert, T., Heckmann, M. B., Rapti, K., Schultheis, D., Jungmann, A., Katus, H. A., Winter, L., Frey, N., Clemen, C. S., Schröder, R., Müller, O. J.
Publicado en Gene Ther (2020)

AAV9-mediated gene transfer of desmin ameliorates cardiomyopathy in desmin-deficient mice

por Heckmann, M B, Bauer, R, Jungmann, A, Winter, L, Rapti, K, Strucksberg, K-H, Clemen, C S, Li, Z, Schröder, R, Katus, H A, Müller, O J
Publicado en Gene Ther (2016)