Duchenne muscular dystrophy (DMD) is caused by frameshift mutations in the DMD gene
that prevent the body-wide translation of its protein product, dystrophin. Besides a severe …

Dystrophin Dp71 is expressed in all tissues, with the exception of skeletal muscle, and is the
main Duchenne muscular dystrophy (DMD) gene product in brain. As full-length dystrophin …

Background Duchenne muscular dystrophy (DMD) is caused by deficient expression of the
cytoskeletal protein, dystrophin. One third of DMD patients also have mental retardation …

Background Duchenne muscular dystrophy (DMD) is caused by DMD mutations leading to
dystrophin loss. Full‐length Dp427 is the primary dystrophin isoform expressed in muscle …

Duchenne muscular dystrophy is a multifactorial disease including a cognitive phenotype. It
is caused by mutations in the X-chromosomal DMD gene from which dystrophin is …

Mental retardation is a clinical feature present in both Duchenne and Becker muscular
dystrophy patients and its pathogenesis is still unknown. Dp140 is a dystrophin isoform with …

Duchenne muscular dystrophy (DMD) is a muscular dystrophy with high incidence of
learning and behavioural problems and is associated with neurodevelopmental disorders …

Duchenne muscular dystrophy (DMD) is a progressive degenerative lethal muscle disease.
A significant proportion of DMD affected children suffer also from mental retardation. The rod …

Several forms of inherited muscular dystrophy are associated with brain abnormalities and
cognitive impairment. One of the most common and severe of these diseases is Duchenne …

The presence of variable degrees of cognitive impairment, extending from severe mental
retardation to specific deficits, in patients with dystrophinopathies is a well-recognized …