Duchenne muscular dystrophy (DMD), caused by mutations in the dystrophin gene, is an X‐
linked disease affecting male and rarely adult heterozygous females, resulting in death by …

Duchenne muscular dystrophy (DMD) is an X‐linked progressive muscle degenerative
disease, caused by mutations in the dystrophin gene and resulting in death because of …

Background Although cardiomyopathy has emerged as a leading cause of death in
Duchenne muscular dystrophy (DMD), limited studies and therapies have emerged for …

Duchenne muscular dystrophy (DMD) is caused by mutations in the dystrophin gene and
dilated cardiomyopathy (DCM) is a major cause of morbidity and mortality in DMD patients …

Duchenne muscular dystrophy (DMD) is a severe genetic disorder characterized by the lack
of functional dystrophin. DMD is associated with progressive dilated cardiomyopathy …

Duchenne muscular dystrophy (DMD) is caused by mutations in the DMD gene which
encodes dystrophin protein. Dystrophin defect affects cardiac muscle as well as skeletal …

Duchenne muscular dystrophy (DMD) is caused by mutations in the dystrophin gene (DMD),
and is characterized by progressive weakness in skeletal and cardiac muscles. Currently …

Duchenne muscular dystrophy (DMD) is a devastating muscle disorder caused by frameshift
mutations in the DMD gene. DMD involves cardiac muscle, and the presence of ventricular …

Duchenne muscular dystrophy (DMD) is the most common and severe form of muscular
dystrophy. The major symptoms of this condition are walking difficulties, dyspnea caused by …

Duchenne muscular dystrophy (DMD) is a progressive and fatal muscle degenerating
disease caused by a dystrophin deficiency. Effective suppression of the primary pathology …