Induced pluripotent stem cells and genome editing technology as therapeutic strategies for Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is a rare genetic, progressive and devastating skeletal and cardiac muscle disorder due to mutation of the dystrophin gene that affects 1 in 3500 young males. Currently, there is no curative management for this pathology. The development of inducedpluripotent stem c...
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Format: | Article |
Language: | English |
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Universitas Gadjah Mada
2021-01-01
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Series: | Journal of the Medical Sciences |
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Online Access: | https://jurnal.ugm.ac.id/bik/article/view/57339 |