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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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Detalhes bibliográficos
Publicado no:J Clin Immunol
Main Authors: Foley, Corinne L., Al Remeithi, Sareea S., Towe, Christopher T., Dauber, Andrew, Backeljauw, Philippe F, Tyzinski, Leah, Kumar, Ashish R., Hwa, Vivian
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
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Acesso em linha: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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