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Human severe combined immunodeficiency: Genetic, phenotypic, and functional diversity in one hundred eight infants

The Journal of Pediatrics · 1997 · Vol. 130(3) · pp. 378–387
Immunodeficiency and Autoimmune DisordersImmune Cell Function and InteractionCytomegalovirus and herpesvirus researchSevere combined immunodeficiencyJanus kinase 3MedicineImmunologyCommon gamma chainImmunodeficiencyPrimary immunodeficiencyPhenotypeMutationBiology
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Human severe combined immunodeficiency: Genetic, phenotypic, and functional diversity in one hundred eight infants · Scinovex