• control
• Pharmacology
• June 12, 2024

Investigating the potential of CRISPR-based gene therapy for the treatment of Duchenne muscular dystrophy – Complete Phd and Masters Thesis

[ad_1] Introduction Duchenne muscular dystrophy (DMD) is a devastating genetic disorder characterized by progressive muscle degeneration and weakness, ultimately leading to loss of ambulation and premature death in affected individuals. Although there is currently no…