Development of an AAV DNA-based synthetic vector for the potential gene therapy of hemophilia in children.

Shoti, Jakob; Qing, Keyun; Srivastava, Arun

Shoti, Jakob; Qing, Keyun; Srivastava, Arun.

Afiliación

Shoti J; Division of Cellular and Molecular Therapy, Department of Pediatrics, University of Florida College of Medicine, Gainesville, FL, United States.
Qing K; Powell Gene Therapy Center, University of Florida College of Medicine, Gainesville, FL, United States.
Srivastava A; Division of Cellular and Molecular Therapy, Department of Pediatrics, University of Florida College of Medicine, Gainesville, FL, United States.

Front Microbiol ; 13: 1033615, 2022.

Article en En | MEDLINE | ID: mdl-36274690

Palabras clave

AAV; AAV vectors; gene therapy; hemophilia; inverted terminal repeats

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Microbiol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza

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