A Novel RFXANK Mutation in a Chinese Child With MHC II Deficiency: Case Report and Literature Review
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DOI: 10.1093/ofid/ofaa314
Abstract: Abstract Major histocompatibility complex (MHC) II deficiency is a rare primary immunodeficiency disorder that is characterized by the deficiency of MHC class II molecules. The disease is caused by transcription factor mutations including class II… read more here.
Keywords: rfxank gene; deficiency; mutation; mhc deficiency ... See more keywords