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455 Ferroptosis in Duchenne muscular dystrophy Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder caused by mutations in dystrophin protein encoded by the DMD gene

10.15167/2421-4248/jpmh2022.63.2S3.2752 244

V vy, bn nn kim tra kh nng kch ng ca sn phm trn mt vng da nh m bo sn phm hp vi da trc khi s dng cho ton khun mt

PMID: 34827486 Dihexa purchased from MedChemExpress

Cardiovasc Res (1994) 28:167985

Early Treatment Diabetic Retinopathy Study research group
