Bowen–Conradi syndrome is a disease in humans that can affect children.[2] The disease is due to an autosomal recessive abnormality of the EMG1gene, which plays a role in small ribosomal subunit (SSU) assembly.[1][3] The preponderance of diagnoses has been in North American Hutterite children, but BWCNS can affect other population groups.[2][4]
^Armistead J, Patel N, Wu X, et al. (2015). "Growth arrest in the ribosomopathy, Bowen-Conradi syndrome, is due to dramatically reduced cell proliferation and a defect in mitotic progression". Biochim. Biophys. Acta. 1852 (5): 1029–37. doi:10.1016/j.bbadis.2015.02.007. PMID25708872.