6533b824fe1ef96bd127ff38

RESEARCH PRODUCT

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

José M. MartínCarlos MonteagudoRebeca VelascoAndrea EstébanezAna CuestaEsmeralda SilvaJaime Verdú-amorós

subject

GeneticsRAG2medicineDermatologyBiologymedicine.diseaseGeneOmenn syndromeHeterozygous mutationhttps://doi.org/10.1111/ddg.14383