Characterization of two iPSC lines from patients with maternally inherited leigh (MILS) and neuropathy, ataxia, and retinitis pigmentosa (NARP) syndrome carrying the MT-ATP6 m.8993 T>G mutation at different degrees of heteroplasmy
Haschke, Anna Maria, Diecke, Sebastian, Schuelke, Markus
Published in Stem cell research (01.12.2024)
Published in Stem cell research (01.12.2024)
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