Highly-Evolved Novel AAV Gene Therapy Directly Addresses Fabry Disease Pathology In Vivo by Cell Autonomous Expression in the Heart and Other Target Organs
/wp-content/uploads/4dmt_logo.svg00Maria Gonzalez/wp-content/uploads/4dmt_logo.svgMaria Gonzalez2023-03-13 16:34:582023-03-13 16:41:53Highly-Evolved Novel AAV Gene Therapy Directly Addresses Fabry Disease Pathology In Vivo by Cell Autonomous Expression in the Heart and Other Target Organs