July 31, 2026 — RNews

#cardiomyocyte — Friday, July 31, 2026 (1 items)

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Phenotype rescue through the restoration of full-length dystrophin using CRISPR/Cas9 genome editing in Duchenne muscular dystrophy patient-derived iPSCs carrying the deletion of two exons. (link.springer.com)

Rovina D … Maione AS Genome Medicine 2026-07-31

#crispr #muscular dystrophy #ipscs #gene therapy #cardiomyocyte