1. Bilginer, Y., Düzova, A., Topaloğlu, R., Batu, E.D., Boduroğlu, K., Güçer, Ş., et al. (2016). Three cases of spondyloenchondrodysplasia (SPENCD) with systemic lupus erythematosus: a case series and review of the literature. Lupus, [online] 25(7), pp.760–765. doi: 10.1177/0961203316629000. Available at: https://pubmed.ncbi.nlm.nih.gov/26854080/.
2. Hong, S.W., Huh, K.-H., Lee, J.K. and Kang, J.-H. (2018). Craniofacial anomalies associated with spondyloenchondrodysplasia. Medicine, [online] 97(50). doi: 10.1097/MD.0000000000013644. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320149/.
3. Girschick, H., Wolf, C., Morbach, H., Hertzberg, C. and Lee-Kirsch, M.A. (2015). Severe immune dysregulation with neurological impairment and minor bone changes in a child with spondyloenchondrodysplasia due to two novel mutations in the ACP5 gene. Pediatric Rheumatology, 13(1). doi: 10.1186/s12969-015-0035-7. Available at: https://ped-rheum.biomedcentral.com/articles/10.1186/s12969-015-0035-7
4. Kara, B., Ekinci, Z., Sahin, S., Gungor, M., Gunes, A.S., Ozturk, K., et al. (2020). Monogenic lupus due to spondyloenchondrodysplasia with spastic paraparesis and intracranial calcification: case-based review. Rheumatology International, 40(11), pp.1903–1910. doi: 10.1007/s00296-020-04653-x. Available at: https://link.springer.com/article/10.1007/s00296-020-04653-x
5. Briggs, T.A., Rice, G.I., Adib, N., Ades, L., Barete, S., Baskar, K., Baudouin, V., Cebeci, A.N., Clapuyt, P., Coman, D., De Somer, L., Finezilber, Y., Frydman, M., Guven, A., Heritier, S., Karall, D., Kulkarni, M.L., Lebon, P., Levitt, D. and Le Merrer, M. (2016). Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey. Journal of Clinical Immunology, [online] 36, pp.220–234. doi: 10.1007/s10875-016-0252-y. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792361/.