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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Formato: | Libro |
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Galenos Yayinevi,
2024-06-01T00:00:00Z.
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Acceso en línea: | Connect to this object online. |
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Número de Clasificación: |
A1234.567 |
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