AAV-mediated gene therapy in Dystrophin-Dp71 deficient mouse leads to blood-retinal barrier restoration and oedema reabsorption.
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J. Sahel | D. Dalkara | R. Tadayoni | M. Pâques | A. Sène | O. Vacca | A. Giocanti-Aurégan | C. Montañez | Hugo Charles-Messance | Á. Rendón | Peggy Barbe | Stéphane Fouquet | Jorge Aragón | Marie Darche | Brahim El Mathari | A. Séne | A. Rendon