Dysregulation of GSK3β-Target Proteins in Skin Fibroblasts of Myotonic Dystrophy Type 1 (DM1) Patients.
Sign Up to like & getrecommendations! Published in 2021 at "Journal of neuromuscular diseases"
DOI: 10.3233/jnd-200558
Abstract: Myotonic dystrophy type 1 (DM1) is the most common monogenetic muscular disorder of adulthood. This multisystemic disease is caused by CTG repeat expansion in the 3'-untranslated region of the DM1 protein kinase gene called DMPK.… read more here.
Keywords: type dm1; dm1; dystrophy type; dm1 patients ... See more keywords