Lagresle-Peyrou, C., Olichon, A., Sadek, H., Roche, P., Tardy, C., Da Silva, C., Garrigue, A., Fischer, A., Moshous, D., Collette, Y., Picard, C., Casanova, J. L., André, I. and Cavazzana, M. (2021) “A gain-of-function RAC2 mutation is associated with bone-marrow hypoplasia and an autosomal dominant form of severe combined immunodeficiency”, Haematologica. Pavia, Italy, 106(2), pp. 404-411. doi: 10.3324/haematol.2019.230250.