A heterozygous mutation in the RAG2 gene with cutaneous and systemic manifestations partially resembling Omenn syndrome
Por:
Estebanez A, Verdu-Amoros J, Silva E, Velasco R, Cuesta A, Monteagudo C, Martin J
Publicada:
1 jun 2021
Ahead of Print:
1 jun 2021
Resumen:
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