Ashish, A., S. Mishra, R. Singh, and S. Rai. “Clinical exome sequencing (carrier screening) identifies the gene INPPL1 in a sporadic case of opsismodysplasia”. European Journal of Clinical and Experimental Medicine, vol. 23, no. 1, Mar. 2025, pp. 277–282, doi:10.15584/ejcem.2025.1.32.