1. Jacob, Prince, Lindelöf, Hillevi, Rustad, Cecilie F, Girisha, Katta M, Grigelioniene, Giedre. 2023. Clinical, genetic and structural delineation of RPL13-related spondyloepimetaphyseal dysplasia suggest extra-ribosomal functions of eL13. In NPJ genomic medicine, 8, 39. doi:10.1038/s41525-023-00380-x. https://pubmed.ncbi.nlm.nih.gov/37993442/
2. Schroeder, Analyne M, Allahyari, Massoud, Vogler, Georg, Grossfeld, Paul, Bodmer, Rolf. . Model system identification of novel congenital heart disease gene candidates: focus on RPL13. In Human molecular genetics, 28, 3954-3969. doi:10.1093/hmg/ddz213. https://pubmed.ncbi.nlm.nih.gov/31625562/
3. Díaz-González, Francisca, Parrón-Pajares, Manuel, Lucas-Castro, Elsa, Sousa, Sergio B, Heath, Karen E. 2023. Evolution of clinical and radiological presentations of spondyloepimetaphyseal dysplasia, RPL13-related: Description of 11 further cases. In Clinical genetics, 104, 100-106. doi:10.1111/cge.14351. https://pubmed.ncbi.nlm.nih.gov/37121912/
4. Luan, Yizhao, Tang, Nan, Yang, Jiaqi, Ju, Rong, Xie, Zhi. . Deficiency of ribosomal proteins reshapes the transcriptional and translational landscape in human cells. In Nucleic acids research, 50, 6601-6617. doi:10.1093/nar/gkac053. https://pubmed.ncbi.nlm.nih.gov/35137207/
5. Le Caignec, Cedric, Ory, Benjamin, Lamoureux, François, Baud'huin, Marc, Isidor, Bertrand. 2019. RPL13 Variants Cause Spondyloepimetaphyseal Dysplasia with Severe Short Stature. In American journal of human genetics, 105, 1040-1047. doi:10.1016/j.ajhg.2019.09.024. https://pubmed.ncbi.nlm.nih.gov/31630789/
智鼠故事 
