Whole‐exome sequencing of T‐B+ severe combined immunodeficiency in Egyptian infants, JAK3 predominance and novel variants

Citation:
Hawary, E. R., S. Meshaal, A. A. Mauracher, L. Opitz, A. D. Elaziz, S. Lotfy, A. Eldash, J. Boutros, N. Galal, P. J. Schmid, et al., "Whole‐exome sequencing of T‐B+ severe combined immunodeficiency in Egyptian infants, JAK3 predominance and novel variants", Clinical and experimental immunology, vol. 203, issue 3, pp. 448-457, 2021.