The ICF2 gene Zbtb24 specifically regulates the differentiation of B1 cells via promoting heme synthesis
Abstract Background Loss-of-function mutations of ZBTB24 cause immunodeficiency, centromeric instability, and facial anomalies syndrome 2 (ICF2). ICF2 is a rare autosomal recessive disorder with immunological defects in serum antibodies and circulating memory B cells, resulting in recurrent and some...
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| Principais autores: | , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BMC
2024-09-01
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| Serier: | Cellular & Molecular Biology Letters |
| Fag: | |
| Online adgang: | https://doi.org/10.1186/s11658-024-00641-2 |
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