Entrada Therapeutics | Myotonic Dystrophy Type 1 (DM1)
Myotonic dystrophy - Wikipedia
Myopathies without EOM Weakness: Facioscapulohumeral + Myotonic Dystrophy
Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2 | European Journal of Human Genetics
Specific DMPK-promoter targeting by CRISPRi reverses myotonic dystrophy type 1-associated defects in patient muscle cells: Molecular Therapy - Nucleic Acids
Frontiers | Muscle wasting in myotonic dystrophies: a model of premature aging
Model for the molecular consequences of triplet expansion in DM1. In... | Download Scientific Diagram