WHIM syndrome: Immunopathogenesis, treatment and cure strategies
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DOI: 10.1111/imr.12719
Abstract: WHIM syndrome is a rare, autosomal dominant immunodeficiency which is named for the four key manifestations: Warts, Hypogammaglobulinemia, Infections, and Myelokathexis. It results from heterozygous gain‐of‐function mutations in the chemokine receptor CXCR4 which is widely… read more here.
Keywords: syndrome immunopathogenesis; whim syndrome; immunopathogenesis treatment; cure strategies ... See more keywords