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Kamilaris, Andrew
Improving the value of clinical research through the use of Common Data Elements.
Alpha-1 Antitrypsin Deficiency as a Candidate for Gene Editing.
CNS-restricted Transduction and CRISPR/Cas9-mediated Gene Deletion with an Engineered AAV Vector.
CRISPR-Based Therapeutic Genome Editing: Strategies and In?Vivo Delivery by AAV Vectors.
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CRISPR-Based Therapeutic Genome Editing: Strategies and In?Vivo Delivery by AAV Vectors.
Wang D, Zhang F, Gao G. CRISPR-Based Therapeutic Genome Editing: Strategies and In?Vivo Delivery by AAV Vectors. Cell. 2020 04 02; 181(1):136-150.
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subject areas
Animals
CRISPR-Cas Systems
Dependovirus
Gene Editing
Genetic Therapy
Genetic Vectors
Humans
authors with profiles
Dan Wang PhD
Guangping Gao PhD