Condition: IMMUNODEFICIENCY 32B


rs397514710 in IRF8 gene and IMMUNODEFICIENCY 32B PMID 25122610 2014 Functional characterization of the human dendritic cell immunodeficiency associated with the IRF8(K108E) mutation.

PMID 21524210 2011 IRF8 mutations and human dendritic-cell immunodeficiency.