1. Halevy, Ayelet, Lerer, Israela, Cohen, Rony, Straussberg, Rachel, Lossos, Alexander. 2014. Novel EXOSC3 mutation causes complicated hereditary spastic paraplegia. In Journal of neurology, 261, 2165-9. doi:10.1007/s00415-014-7457-x. https://pubmed.ncbi.nlm.nih.gov/25149867/
2. Wan, Jijun, Yourshaw, Michael, Mamsa, Hafsa, Nelson, Stanley F, Jen, Joanna C. 2012. Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration. In Nature genetics, 44, 704-8. doi:10.1038/ng.2254. https://pubmed.ncbi.nlm.nih.gov/22544365/
3. de Amorim, Julia L, Leung, Sara W, Haji-Seyed-Javadi, Ramona, Yao, Bing, Corbett, Anita H. 2024. The putative RNA helicase DDX1 associates with the nuclear RNA exosome and modulates RNA/DNA hybrids (R-loops). In The Journal of biological chemistry, 300, 105646. doi:10.1016/j.jbc.2024.105646. https://pubmed.ncbi.nlm.nih.gov/38219817/
4. Stansfield, Ben N, Rangasamy, Sampath, Ramsey, Keri, Khanna, May, Churko, Jared M. 2022. Generation of an iPSC line from a Pontocerebellar Hypoplasia 1B patient harboring a homozygous c.395 A > C mutation in EXOSC3 along with a family matched control. In Stem cell research, 65, 102944. doi:10.1016/j.scr.2022.102944. https://pubmed.ncbi.nlm.nih.gov/36257093/