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-amoróssubject
GeneticsRAG2medicineDermatologyBiologymedicine.diseaseGeneOmenn syndromeHeterozygous mutationyear | journal | country | edition | language |
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2021-06-01 | JDDG: Journal der Deutschen Dermatologischen Gesellschaft |