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CRISPR-Cas Gene Editing Delivery Vector for Targeted Neural Tissue Therapeutic Intervention

Patent #US11999402B2

A synthetic viral vector designed for site-specific delivery of genetic editing components into central nervous system tissues. The invention allows for enhanced blood-brain barrier penetration without inducing adverse immune responses.

Issue Date

5/1/2026

Inventor

Dr. Sarah Jenkins

Seller Location

United States

Price on request

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