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What is Molecular Mechanism of Duchenne Muscular Dystrophy about?

Duchenne muscular dystrophy (DMD) is caused by mutations in the dystrophin gene, leading to muscle degeneration and loss of function. Various therapeutic approaches, including gene correction and the use of aminoglycoside antibiotics, show promise but have not yet achieved significant success in human studies. The disease primarily affects males and results in severe muscle weakness, with patients typically becoming wheelchair-bound by age 12 and facing life-threatening complications in their late teens or

Author

roshanali7gtk

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EN