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

Autor: Maxime R. F. Gosselin, Etienne Kornobis, Jean-Baptiste Dupont, Spiros D. Garbis, Christian Pinset, Alan R L Dorval, Antigoni Manousopoulou, Virginie Mournetas, Margot Jarrige, Dariusz C. Górecki, Hélène Polvèche, Emmanuelle Massouridès

Publikováno v: Mournetas, V, Massouridès, E, Dupont, JB, Kornobis, E, Polvèche, H, Jarrige, M, Dorval, A R L, Gosselin, M R F, Manousopoulou, A, Garbis, S D, Górecki, D C & Pinset, C 2021, ' Myogenesis modelled by human pluripotent stem cells: a multi-omic study of Duchenne myopathy early onset ', Journal of Cachexia, Sarcopenia and Muscle, vol. 12, no. 1, pp. 209-232 . https://doi.org/10.1002/jcsm.12665
Journal of Cachexia, Sarcopenia and Muscle
Journal of Cachexia, Sarcopenia and Muscle, 2021, 12 (1), pp.209-232. ⟨10.1002/jcsm.12665⟩
Journal of Cachexia, Sarcopenia and Muscle, Vol 12, Iss 1, Pp 209-232 (2021)

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 t

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https://researchportal.port.ac.uk/ws/files/27071227/Myogenesis_modelled_by_human_pluripotent_stem_cells.pdf