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穿孔素基因缺陷原发性噬血细胞综合征的临床特征：单中心回顾性研究
OBJECTIVE: This study aimed to investigate the clinical characteristics of patients diagnosed with primary hemophagocytic lymphohistiocytosis（pHLH）associated with perforin gene deficiency. METHODS: We retrospectively analyzed the clinical data of 16 pHLH patients associated with perforin gene defici...
| Formato: | Online Artículo Texto |
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| Lenguaje: | English |
| Publicado: |
Editorial office of Chinese Journal of Hematology
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509624/ https://www.ncbi.nlm.nih.gov/pubmed/37749038 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2023.07.009 |