1. Fortuna, Tyler R, Kour, Sukhleen, Chimata, Anuradha Venkatakrishnan, Singh, Amit, Pandey, Udai Bhan. 2023. SMN regulates GEMIN5 expression and acts as a modifier of GEMIN5-mediated neurodegeneration. In Acta neuropathologica, 146, 477-498. doi:10.1007/s00401-023-02607-8. https://pubmed.ncbi.nlm.nih.gov/37369805/
2. Kour, Sukhleen, Rajan, Deepa S, Fortuna, Tyler R, Senderek, Jan, Pandey, Udai Bhan. 2021. Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder. In Nature communications, 12, 2558. doi:10.1038/s41467-021-22627-w. https://pubmed.ncbi.nlm.nih.gov/33963192/
3. Cascajo-Almenara, Marivi V, Juliá-Palacios, Natalia, Urreizti, Roser, Santos-Ocaña, Carlos, Artuch, Rafael. 2024. Mutations of GEMIN5 are associated with coenzyme Q10 deficiency: long-term follow-up after treatment. In European journal of human genetics : EJHG, 32, 426-434. doi:10.1038/s41431-023-01526-2. https://pubmed.ncbi.nlm.nih.gov/38316953/
4. Francisco-Velilla, Rosario, Embarc-Buh, Azman, Del Caño-Ochoa, Francisco, Ramón-Maiques, Santiago, Martinez-Salas, Encarnacion. 2022. Functional and structural deficiencies of Gemin5 variants associated with neurological disorders. In Life science alliance, 5, . doi:10.26508/lsa.202201403. https://pubmed.ncbi.nlm.nih.gov/35393353/
5. Liu, Xiaofen, Zhang, Wenjuan, Jing, Changbin, Pan, Weijun, Li, Dantong. 2021. Mutation of Gemin5 Causes Defective Hematopoietic Stem/Progenitor Cells Proliferation in Zebrafish Embryonic Hematopoiesis. In Frontiers in cell and developmental biology, 9, 670654. doi:10.3389/fcell.2021.670654. https://pubmed.ncbi.nlm.nih.gov/33996826/