Human iPSC disease modelling reveals functional and structural defects in retinal pigment epithelial cells harbouring the m.3243A > G mitochondrial DNA mutation
Valeria Chichagova(Newcastle University), David Steel(Sunderland Eye Infirmary), Dean Hallam(Newcastle University), Lyle Armstrong(Newcastle University), Gabriele Saretzki(Newcastle University), Adriana Buskin(Newcastle University), Patrick Yu‐Wai‐Man(Moorfields Eye Hospital NHS Foundation Trust), Joseph Collin(Newcastle University), Majlinda Lako(Newcastle University)
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