Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients

• Autores principales: Handan Duman Şenol (Autor), Meral Barlık (Autor), Ezgi Topyıldız (Autor), Figen Gülen (Autor), Güzide Aksu (Autor), Necil Kütükçüler (Autor), Esen Demir (Autor), Neslihan Edeer Karaca (Autor)
• Formato: Libro
• Publicado: Galenos Yayinevi, 2024-06-01T00:00:00Z.
• Materias: article
• Acceso en línea: Connect to this object online.

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...