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Developmental adaptive immune defects associated with STAT5B deficiency in three young siblings
Patients with rare homozygous mutations in signal transducer and activator of transcription 5B (STAT5B) develop immunodeficiency resulting in chronic eczema, chronic infections, autoimmunity, and chronic lung disease. STAT5B deficient patients are typically diagnosed in the teenage years, limiting o...
Guardat en:
| Publicat a: | J Clin Immunol |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7854992/ https://ncbi.nlm.nih.gov/pubmed/33090292 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10875-020-00884-6 |
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