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

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

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...

Full description

Bibliographic Details
Main Authors: Virginie Mournetas, Emmanuelle Massouridès, Jean‐Baptiste Dupont, Etienne Kornobis, Hélène Polvèche, Margot Jarrige, Alan R.L. Dorval, Maxime R.F. Gosselin, Antigoni Manousopoulou, Spiros D. Garbis, Dariusz C. Górecki, Christian Pinset
Format: Article
Language:English
Published: Wiley 2021-02-01
Series:Journal of Cachexia, Sarcopenia and Muscle
Subjects:
Duchenne muscular dystrophy
Myogenesis
Human pluripotent stem cells
Omics
Online Access:https://doi.org/10.1002/jcsm.12665

Similar Items

Similar Items