1. Sager, Gunes, Turkyilmaz, Ayberk, Ates, Esra Arslan, Kutlubay, Busra. 2021. HACE1, GLRX5, and ELP2 gene variant cause spastic paraplegies. In Acta neurologica Belgica, 122, 391-399. doi:10.1007/s13760-021-01649-7. https://pubmed.ncbi.nlm.nih.gov/33813722/
2. Russo, Angelo, Forest, Cristina, Leone, Giulia Joy, Cordelli, Duccio Maria, Suppiej, Agnese. 2021. ELP2 compound heterozygous variants associated with cortico-cerebellar atrophy, nodular heterotopia and epilepsy: Phenotype expansion and review of the literature. In European journal of medical genetics, 64, 104361. doi:10.1016/j.ejmg.2021.104361. https://pubmed.ncbi.nlm.nih.gov/34653680/
3. Fellows, J, Erdjument-Bromage, H, Tempst, P, Svejstrup, J Q. . The Elp2 subunit of elongator and elongating RNA polymerase II holoenzyme is a WD40 repeat protein. In The Journal of biological chemistry, 275, 12896-9. doi:. https://pubmed.ncbi.nlm.nih.gov/10777588/