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...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2023
Materias:
论著
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

Internet

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

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