IL-7 receptor deficient SCID with a unique intronic mutation and post-transplant autoimmunity due to chronic GVHD

Clinical Immunology

Volumn 125, Issue 2, 2007, Pages 159-164

  Butte, Manish J ^a,b   Haines, Charles ^c   Bonilla, Francisco A ^b   Puck, Jennifer ^d  

^a HARVARD MEDICAL SCHOOL   (United States)

^b BOSTON CHILDREN S HOSPITAL   (United States)

^c JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Hematopoietic stem cell transplantation; HSCT; Human mutation; Interleukin 7 receptor; Intronic mutation; Mechanisms of mutation; Myasthenia gravis; Myositis; SCID; Severe combined immunodeficiency

Indexed keywords

CYTOKINE; CYTOKINE RECEPTOR; INTERLEUKIN 7 RECEPTOR; MESSENGER RNA;

ALLELE; ARTICLE; AUTOIMMUNITY; CASE REPORT; CELL DIFFERENTIATION; CHRONIC GRAFT VERSUS HOST DISEASE; CLINICAL FEATURE; COMBINED IMMUNODEFICIENCY; EXON; GENE; GENE MUTATION; GENETIC DISORDER; HEMATOPOIETIC STEM CELL TRANSPLANTATION; HUMAN; HUMAN TISSUE; IL7R GENE; INFANT; INTRON; MALE; MYASTHENIA GRAVIS; MYOSITIS; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRESCHOOL CHILD; PRIORITY JOURNAL; T LYMPHOCYTE;

BASE SEQUENCE; GRAFT VS HOST DISEASE; HEMATOPOIETIC STEM CELL TRANSPLANTATION; HUMANS; INFANT; INTRONS; MALE; MYASTHENIA GRAVIS; MYOSITIS; POINT MUTATION; RECEPTORS, INTERLEUKIN-7; SEVERE COMBINED IMMUNODEFICIENCY;

EID: 35348842896     PISSN: 15216616     EISSN: 15217035     Source Type: Journal    
DOI: 10.1016/j.clim.2007.06.007     Document Type: Article

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