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AAV-mediated gene therapy in Dystrophin-Dp71 deficient mous..:
Vacca, Ophélie
;
Charles-Messance, Hugo
;
El Mathari, Brahim
...
Human Molecular Genetics. , 2016
Link:
https://doi.org/10.1093/hmg/ddw159
RT Journal T1
AAV-mediated gene therapy in Dystrophin-Dp71 deficient mouse leads to blood-retinal barrier restoration and oedema reabsorption
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddw159&Exemplar=1&LAN=DE A1 Vacca, Ophélie A1 Charles-Messance, Hugo A1 El Mathari, Brahim A1 Sene, Abdoulaye A1 Barbe, Peggy A1 Fouquet, Stéphane A1 Aragón, Jorge A1 Darche, Marie A1 Giocanti-Aurégan, Audrey A1 Paques, Michel A1 Sahel, José-Alain A1 Tadayoni, Ramin A1 Montañez, Cecilia A1 Dalkara, Deniz A1 Rendon, Alvaro PB Oxford University Press (OUP) YR 2016 SN 0964-6906 SN 1460-2083 JF Human Molecular Genetics SP ddw159 LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddw159 DO https://doi.org/10.1093/hmg/ddw159 SF ELIB - SuUB Bremen
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