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A101 ARPC1B-DEFICIENT B CELLS DISPLAY ABERRANT SPREADING BEHAVIOUR
BACKGROUND: ARPC1B-deficiency is a newly described genetic condition with an early age of onset and is clinically similar to Wiskott-Aldrich syndrome (WAS). Nearly all affected patients experience colitis that is eosinophilic in nature, and their immunological profiles show increased peripheral CD19...
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| Pubblicato in: | J Can Assoc Gastroenterol |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6508295/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jcag/gwy009.101 |
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