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Functional Characterization of a Homozygous TRAF6 Mutation Causing NF-κB Signaling Defects and Human Immunodeficiency Disease
DownloadFall 2018
As many as 80,000 Albertans are affected by rare diseases; with the greatest prevalence in children such diseases dramatically impact the lives of both those suffering and the families caring for them. Severe combined immunodeficiency (SCID) represents a group of inherited disorders characterized...
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