LAUSR

Limited role of interferon‐kappa (IFNK) truncating mutations in common variable immunodeficiency

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0 Published in 2017 at "Cytokine"

DOI: 10.1016/j.cyto.2017.03.005

Abstract: HighlightsWhole exome sequencing was performed to determine the genetic background of common variable immunodeficiency in two non‐consanguineous German families.IFNK was found as the only candidate gene that harbored truncating mutations in affected members from both… read more here.

Keywords: variable immunodeficiency; truncating mutations; common variable; ifnk ... See more keywords