Myogenesis modelled by human pluripotent stem cells: a multi‐omic study of Duchenne myopathy early onset

• Prif Awduron: Virginie Mournetas (Awdur), Emmanuelle Massouridès (Awdur), Jean‐Baptiste Dupont (Awdur), Etienne Kornobis (Awdur), Hélène Polvèche (Awdur), Margot Jarrige (Awdur), Alan R.L. Dorval (Awdur), Maxime R.F. Gosselin (Awdur), Antigoni Manousopoulou (Awdur), Spiros D. Garbis (Awdur), Dariusz C. Górecki (Awdur), Christian Pinset (Awdur)
• Fformat: Llyfr
• Cyhoeddwyd: Wiley, 2021-02-01T00:00:00Z.
• Pynciau: article
• Mynediad Ar-lein: Connect to this object online.

Abstract Background Duchenne muscular dystrophy (DMD) causes severe disability of children and death of young men, with an incidence of approximately 1/5000 male births. Symptoms appear in early childhood, with a diagnosis made mostly around 4 years old, a time where the amount of muscle damage is a...