A heterozygous mutation in the RAG2 gene with cutaneous and systemic manifestations partially resembling Omenn syndrome

1. Estébanez, A.
2. Verdú-Amorós, J.
3. Silva, E.
4. Velasco, R.
5. Cuesta, A.
6. Monteagudo, C.
7. Martín, J.M.