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Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study
BACKGROUND: Immunodysregulation polyendocrinopathy enteropathy x-linked(IPEX) syndromeis a monogenic autoimmune disease caused by FOXP3 mutations. Because it is a rare disease, the natural history and response to treatments, including allogeneic hematopoietic stem cell transplantation (HSCT) and imm...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050203/ https://www.ncbi.nlm.nih.gov/pubmed/29241729 http://dx.doi.org/10.1016/j.jaci.2017.10.041 |