De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosaMathieu Quinodoz, John N. De Roach, Kim Rodenburg et al.|medRxiv|2025Cited by 15
Prime editing for the investigation of aberrant splicing defect associated with a pathogenic PRPH2 variantBruna Lopes da Costa, Peter M. J. Quinn, Siyuan Liu et al.|Molecular Therapy — Nucleic Acids|2025Cited by 3