Functional confirmation of DNA repair defect in ataxia telangiectasia (AT) infants identified by newborn screening for severe combined immunodeficiency (NBS SCID)
The Journal of Allergy and Clinical Immunology: In Practice | Sep 11, 2020
Heritable risk for severe anaphylaxis associated with increased α-tryptase–encoding germline copy number at TPSAB1
The Journal of Allergy and Clinical Immunology | Aug 26, 2020
Most read this week