In Vivo Parieto-Occipital White Matter Metabolism Is Correlated with Visuospatial Deficits in Adult DM1 Patients
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DOI: 10.3390/diagnostics12102305
Abstract: Myotonic dystrophy type 1 (DM1) is a genetic disorder caused by a (CTG) expansion in the DM protein kinase (DMPK) gene, representing the most common adult muscular dystrophy, characterized by a multisystem involvement with predominantly… read more here.
Keywords: matter; matter metabolism; dm1 patients; white matter ... See more keywords