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See Latest ArticlesImmunodeficiency Associated with FCN3 Mutation and Ficolin-3 Deficiency
New England Journal of Medicine, 06/18/09
Munthe-Fog L et al. - The authors describe a patient with recurrent infections who was homozygous for this mutation, who had undetectable serum levels of ficolin-3, and who had a deficiency in ficolin-3–dependent complement activation.
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