Myogenesis Defects in a Patient-Derived iPSC Model of Hereditary GNE Myopathy

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Bob
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Investigators aimed to address this knowledge gap by querying the underlying mechanisms of UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase (GNE) myopathy using a patient-derived iPSC model.
[NPJ Regenerative Medicine]
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