Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients

• Asıl Yazarlar: Handan Duman Şenol (Yazar), Meral Barlık (Yazar), Ezgi Topyıldız (Yazar), Figen Gülen (Yazar), Güzide Aksu (Yazar), Necil Kütükçüler (Yazar), Esen Demir (Yazar), Neslihan Edeer Karaca (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Galenos Yayinevi, 2024-06-01T00:00:00Z.
• Konular: article
• Online Erişim: 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...