Lehalle, D., Mosca-Boidron, A., Begtrup, A., Boute-Benejean, O., Charles, P., Cho, M. T., Clarkson, A., Devinsky, O., Duffourd, Y., Duplomb-Jego, L., Gérard, B., Jacquette, A., Kuentz, P., Masurel-Paulet, A., McDougall, C., Moutton, S., Olivié, H., Park, S., Rauch, A., Revencu, N., Rivière, J., Rubin, K., Simonic, I., Shears, D. J., Smol, T., Taylor Tavares, A. L., Terhal, P., Thevenon, J., Van Gassen, K., Vincent-Delorme, C., Willemsen, M. H., Wilson, G. N., Zackai, E., Zweier, C., Callier, P., Thauvin-Robinet, C., & Faivre, L. (2017). sTAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability. Journal of medical genetics, 54(7), 479–488. http://access.bl.uk/ark:/81055/vdc_100135147747.0x000036