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FOXN1 Gene Considerations in Severe Combined Immunodeficiency Treatment in Children
Forkheadbox N1 (FOXN1) gene mutation in humans is a rare cause of thymic hypoplasia and T cell immunodeficiency. This gene is the master transcriptional regulator of thymic epithelial cells and disruptions have been described in consequence to a variety of antepartum complications. FOXN1 mutation-me...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Cureus
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9800850/ https://www.ncbi.nlm.nih.gov/pubmed/36600823 http://dx.doi.org/10.7759/cureus.32040 |