Another way that scientists propose as a treatment to cure muscular dystrophy is

The correct option is Discovering chemicals which can substitute the missing chemical.

Muscular dystrophy refers to a group of genetic diseases characterized by progressive weakness and degeneration of the skeletal muscles. These disorders are primarily caused by mutations in genes that interfere with the production of proteins, such as dystrophin, which are critical for healthy muscle structure and function.

One of the therapeutic approaches proposed by scientists to treat or manage muscular dystrophy involves identifying and developing chemical compounds or drugs that can bypass or substitute for the missing functional proteins. By discovering chemical substitutes that mimic the role of the missing protein or compensate for its absence, researchers aim to stabilize muscle cell membranes and prevent further degeneration, offering a viable pathway to alleviate the symptoms of the disease.