Items where authors include "O'Callaghan, E."

Conference abstract

Poulter, J., Nadat, F., O'Callaghan, E. et al. (13 more authors) (2024) P13.018.D Biallelic mutation of CWF19L2, encoding a core spliceosome subunit, causes a combined neurodevelopmental and immunodeficiency disorder. [Conference abstract]