Mutant PRPF8 Causes Widespread Splicing Changes in Spliceosome Components in Retinitis Pigmentosa Patient iPSC-Derived RPE Cells

Citation
Arzalluz-Luque, Á., Cabrera, J. L., Skottman, H., Benguria, A., Bolinches-Amorós, A., Cuenca, N., Lupo, V., Dopazo, A., Tarazona, S., Delás, B., Carballo, M., Pascual, B., Hernan, I., Erceg, S., & Lukovic, D. (2021). Mutant PRPF8 Causes Widespread Splicing Changes in Spliceosome Components in Retinitis Pigmentosa Patient iPSC-Derived RPE Cells. Frontiers in Neuroscience, 15. https://doi.org/10.3389/fnins.2021.636969
DOI:
DOI: 10.3389/fnins.2021.636969
Year of publication:
2021
Authors participating in BCBHub:
Ángeles Arzalluz Luque