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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...

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Bibliografiska uppgifter
I publikationen:J Clin Immunol
Huvudupphovsmän: Foley, Corinne L., Al Remeithi, Sareea S., Towe, Christopher T., Dauber, Andrew, Backeljauw, Philippe F, Tyzinski, Leah, Kumar, Ashish R., Hwa, Vivian
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2020
Ämnen:
Länkar: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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