Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients
Aim: Cystic fibrosis (CF) is an autosomal recessive disorder. Although it is considered as an epithelial disease due to impaired chloride transport, its pathogenesis remains unclear. CF is classified as a syndrome with congenital defects of phagocyte in recent human inborn errors of immunity phenoty...
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| Main Authors: | , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Galenos Publishing House
2024-06-01
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| Series: | Journal of Pediatric Research |
| Subjects: | |
| Online Access: | https://jpedres.org/articles/investigation-of-phagocyte-functions-in-pseudomonas-colonized-cystic-fibrosis-patients/doi/jpr.galenos.2024.09735 |
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