Innovative gene therapy ‘reprograms’ cells to reverse neurological deficiencies
French surgeon behind world-first face and hand transplants dies
12 July 2021The first molecular map describing human cerebellar development
12 July 2021Innovative gene therapy ‘reprograms’ cells to reverse neurological deficiencies
A novel method of gene therapy is helping children born with a rare genetic disorder called AADC deficiency that causes severe physical and developmental disabilities. The study, led by researchers at The Ohio State University Wexner Medical Center and The Ohio State University College of Medicine, offers new hope to those living with incurable genetic and neurodegenerative diseases.
