Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients
Volume: 132, Issue: 5, Pages: 1156 - 1163.e5
Published: Nov 1, 2013
Abstract
Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder of phagocytes resulting in impaired killing of bacteria and fungi. A mutation in one of the 4 genes encoding the components p22(phox), p47(phox), p67(phox), and p40(phox) of the leukocyte nicotinamide dinucleotide phosphate reduced (NADPH) oxidase leads to autosomal recessive (AR) CGD. A mutation in the CYBB gene encoding gp91(phox) leads to X-linked recessive...
Paper Details
Title
Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients
Published Date
Nov 1, 2013
Volume
132
Issue
5
Pages
1156 - 1163.e5
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