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2008;283(20):13565-13577.[DOI] 57
ICF syndrome is a rare autosomal recessive disease characterized by facial dysmorphism, immunoglobulin deficiency, IDD, recurrent and prolonged respiratory infections, and infections of the skin and digestive system (Valkova et al., 1987
Activation of GLP-1R by GLP-1 or other exogenous agonists, including exendin-4 and liraglutide, decreases inflammatory responses in several animal models like rat heart and whole animal model
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