X-linked SCID with a rare mutation
Abstract Background Severe combined immunodeficiency (SCID) is a group of relatively rare primary immunodeficiency disorders (PIDs), characterized by disturbed development of T cells and B cells, caused by several genetic mutations that bring on different clinical presentations. SCID may be inherite...
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| Hoofdauteurs: | , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
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BMC
2021-10-01
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| Reeks: | Allergy, Asthma & Clinical Immunology |
| Onderwerpen: | |
| Online toegang: | https://doi.org/10.1186/s13223-021-00605-7 |
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