Clinical, biological and cytometric characteristics of two patients with a homozygous A91V PRF1 mutation
Abstract Objectives Inborn errors of immunity are rare genetic disorders that cause dysfunction of the immune system. Among these, familial haemophagocytic lymphohistiocytosis (FHL) involves defects in the perforin/granzyme pathway, which is essential for regulating immune responses. These condition...
I tiakina i:
| Ngā kaituhi matua: | , , , , , , , , , , , , |
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| Hōputu: | Artigo |
| Reo: | Inglês |
| I whakaputaina: |
Wiley
2026-03-01
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| Rangatū: | Clinical & Translational Immunology |
| Ngā marau: | |
| Urunga tuihono: | https://doi.org/10.1002/cti2.70081 |
| Ngā Tūtohu: |
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
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