Article
Biological and genetic therapies for the treatment of Duchenne muscular dystrophy.
Expert opinion on biological therapy - 1 Jan 2023
Wilton-Clark Harry, Yokota Toshifumi
Abstract excerpt
INTRODUCTION: Duchenne muscular dystrophy is a lethal genetic disease which currently has no cure, and poor standard treatment options largely focused on symptom relief. The development of multiple biological and genetic therapies is underway across various stages of clinical progress which could markedly affect how DMD patients are treated in the future. AREAS COVERED: The purpose of this review is to provide an...
Topics
- Humans
- Muscular Dystrophy, Duchenne
- Dystrophin
- Utrophin
- Genetic Therapy
- Mutation
