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Agammaglobulinemia: from X-linked to Autosomal Forms of Disease
Interruptions or alterations in the B cell development pathway can lead to primary B cell immunodeficiency with resultant absence or diminished immunoglobulin production. While the most common cause of congenital agammaglobulinemia is X-linked agammaglobulinemia (XLA), accounting for approximately 8...
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| Pubblicato in: | Clin Rev Allergy Immunol |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Springer US
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8269404/ https://ncbi.nlm.nih.gov/pubmed/34241796 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12016-021-08870-5 |
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