RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency

Omar K Alkhairy1, Nima Rezaei2, Robert R Graham3

  • 1Division of Clinical Immunology and Transfusion Medicine, Department of Laboratory Medicine, Karolinska Institutet at Karolinska University Hospital Huddinge, Stockholm, Sweden; Department of Pathology and Laboratory Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia.

Abstract

No abstract available in PubMed .

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