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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer US
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8269404/ https://www.ncbi.nlm.nih.gov/pubmed/34241796 http://dx.doi.org/10.1007/s12016-021-08870-5 |