miR‐181a/b downregulation: a mutation‐independent therapeutic approach for inherited retinal diseases
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DOI: 10.15252/emmm.202215941
Abstract: Inherited retinal diseases (IRDs) are a group of diseases whose common landmark is progressive photoreceptor loss. The development of gene‐specific therapies for IRDs is hampered by their wide genetic heterogeneity. Mitochondrial dysfunction is proving to… read more here.
Keywords: mir 181a; inherited retinal; mutation independent; retinal diseases ... See more keywords