Clinical and genetic heterogeneity in Omenn syndrome and severe combined immune deficiency. [electronic resource]
Producer: 20090907Description: 244-50 p. digitalISSN:- 1399-3046
- Cytokines -- genetics
- Exanthema -- genetics
- Female
- Homeodomain Proteins -- genetics
- Humans
- Immunologic Deficiency Syndromes -- complications
- Infant
- Male
- Models, Genetic
- Mutation
- Phenotype
- Severe Combined Immunodeficiency -- complications
- T-Lymphocytes -- metabolism
- Time Factors
- Treatment Outcome
- VDJ Recombinases -- genetics
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Publication Type: Case Reports; Journal Article
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