Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicism

Journal of Allergy and Clinical Immunology

Volumn 131, Issue 6, 2013, Pages 1586-1593

  Hsu, Amy P ^a   Sowerwine, Kathryn J ^a   Lawrence, Monica G ^a   Davis, Joie ^a   Henderson, Carolyn J ^a   Zarember, Kol A ^a   Garofalo, Mary ^a   Gallin, John I ^a   Kuhns, Douglas B ^b   Heller, Theo ^c   Milner, Joshua D ^a   Puck, Jennifer M ^d   Freeman, Alexandra F ^a   Holland, Steven M ^a  

^a NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES   (United States)

^b SAIC FREDERICK INC   (United States)

^c NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

autosomal dominant hyper IgE syndrome; Job syndrome; signal transducer and activator of transcription 3; Somatic mosaicism

Indexed keywords

STAT3 PROTEIN;

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CD8+ T LYMPHOCYTE; CELL COMPARTMENTALIZATION; CONTROLLED STUDY; HUMAN; HUMAN TISSUE; HYPER IGE SYNDROME; MALE; MOLECULAR MECHANICS; MOSAICISM; MUCOCUTANEOUS CANDIDIASIS; NEUTROPHIL; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROGENY; SOMATIC MOSAICISM; TH17 CELL;

ADULT; ALLELES; BASE SEQUENCE; EXONS; HUMANS; JOB'S SYNDROME; MALE; MIDDLE AGED; MOSAICISM; MUTATION; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; STAT3 TRANSCRIPTION FACTOR; TH17 CELLS;

EID: 84878539074     PISSN: 00916749     EISSN: 10976825     Source Type: Journal    
DOI: 10.1016/j.jaci.2013.02.038     Document Type: Article

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