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Gene Therapy for Duchenne Muscular Dystrophy: Unlocking the Opportunities in Countries in the Middle East and Beyond
BACKGROUND: Duchenne muscular dystrophy (DMD) is a severe neuromuscular disorder which leads to progressive muscle degeneration and weakness. Most patients die from cardiac or respiratory failure. Gene transfer therapy offers a promising approach to treating this disorder. OBJECTIVE: Given the genet...
Autores principales: | Elbashir, Haitham, Fathalla, Waseem, Mundada, Vivek, Iqbal, Mehtab, Al Tawari, Asmaa A, Chandratre, Saleel, Bastaki, Laila, Romany, Ingy, Ismayl, Omar, Abou Tayoun, Ahmad |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9697043/ https://www.ncbi.nlm.nih.gov/pubmed/36245386 http://dx.doi.org/10.3233/JND-221528 |
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