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Characterization of 12 AAV Vectors for Intravascular Delivery to Target CNS and Detarget Non-CNS Tissues by MIRNA Regulation: Implications in Treatment of Canavan Disease
Detailed Technology Description
New effective and safe gene therapy approach that allows gene delivery across the blood brain barrier (BBB) upon intravascular administration. Designed to minimize off-target effects by incorporation
Countries
Not Available
Application No.
None
Country/Region
USA
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