RTC 13 effectively counteracts ‘nonsense’ mutation that causes disorder. Scientists at UCLA have identified a new compound that could treat...
Scientists identified a sequence in the dystrophin gene that is essential for helping muscle tissues function, a breakthrough discovery that could lead to treatments for the deadly hereditary disease.
A nationwide clinical trial for a new type treatment that could offer help to those suffering from Duchenne Muscular Dystrophy, a devastating neuromuscular disease.
Researchers have been able to repair a defect responsible for Duchenne muscular dystrophy by using a novel genetic editing technique.
Muscle regeneration in mouse models of Duchenne muscular dystrophy is improved when THI is purified and given in appropriate doses, a new study suggests.
A patient with Duchenne muscular dystrophy is only one of three people in the US to receive a LVAD to keep his weakened heart pumping blood around his body.
Researchers report they have created the first lab grown, contracting human muscles.
A newly developed approach could be used to treat Duchenne muscular dystrophy, researchers believe.
A new study reports on a new method of stem cell transplantation that could help people with Duchenne muscular dystrophy.
The FDA have approved the first drug designed to treat patients with Duchenne muscular dystrophy.
A new study may help to increase understanding of Duchenne muscular dystrophy.
Researchers successfully use CRISPR-Cpf1 to correct Duchenne muscular dystrophy in both animal and human cells.
