DOI: 10.7504/ek2014100608
Variable clinical phenotypes of severe combined immunodeficiency caused by RAG1 mutations
Keywords：RAG1 genesevere combined immunodeficiency diseaseOmenn syndromeautoimmune hemolytic anemia
Publication Date：2014-01-01
Online Publishing Date：2025-08-15(First online date of this platform, not the publication date of the document)