Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy
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DOI: 10.1007/s12035-019-01845-w
Abstract: 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 muscle phenotype, cognitive impairment and neuropsychiatric symptoms are prevalent.… read more here.
Keywords: muscular dystrophy; dp71; dp71 neuropathophysiology; dystrophin ... See more keywords