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AAV-mediated gene therapy in Dystrophin-Dp71 deficient mouse leads to blood-retinal barrier restoration and oedema reabsorption.

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Description scientific article published on 10 June 2016
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author: Ophélie Vacca  Abdoulaye Sene  Peggy Barbe  Brahim El Mathari  Hugo Charles-Messance  Stéphane Fouquet  José-Alain Sahel  Deniz Dalkara 

Publication date June 10, 2016
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