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...

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Vydáno v:J Clin Immunol
Hlavní autoři: Foley, Corinne L., Al Remeithi, Sareea S., Towe, Christopher T., Dauber, Andrew, Backeljauw, Philippe F, Tyzinski, Leah, Kumar, Ashish R., Hwa, Vivian
Médium: Artigo
Jazyk:Inglês
Vydáno: 2020
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Article
On-line přístup: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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