https://pubmed.ncbi.nlm.nih.gov/39932794/
MBNL overexpression rescues cardiac phenotypes in a myotonic dystrophy type 1 heart mouse model
Myotonic dystrophy type 1 (DM1) is an autosomal dominant disease caused by a CTG repeat expansion in the dystrophia myotonica protein kinase (DMPK) gene. The...