Autoimmune lymphoproliferative syndrome-like disease in patients with LRBA mutation

Clinical Immunology

Volumn 159, Issue 1, 2015, Pages 84-92

  Revel Vilk, Shoshana ^a   Fischer, Ute ^b   Keller, Bärbel ^c   Nabhani, Schafiq ^b   Gámez Díaz, Laura ^c   Rensing Ehl, Anne ^c   Gombert, Michael ^b   Hönscheid, Andrea ^b   Saleh, Hani ^d   Shaag, Avraham ^a   Borkhardt, Arndt ^b   Grimbacher, Bodo ^c   Warnatz, Klaus ^c   Elpeleg, Orly ^a   Stepensky, Polina ^a  

^a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^b UNIVERSITY HOSPITAL DÜSSELDORF   (Germany)

^c UNIVERSITY OF FREIBURG   (Germany)

^d Augusta Victoria Hospital   (Israel)

Author keywords

Autoimmune lymphoproliferative disorder; Immunodeficiency

Indexed keywords

GENOMIC DNA; LRBA PROTEIN, HUMAN; SIGNAL TRANSDUCING ADAPTOR PROTEIN;

APOPTOSIS; ARTICLE; AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME; B LYMPHOCYTE; BLOOD SAMPLING; CELL DEATH; CHRONIC LUNG DISEASE; COMBINED IMMUNODEFICIENCY; ENTEROPATHY; EXOME; FLOW CYTOMETRY; GENE MUTATION; GERMLINE MUTATION; HOMEOSTASIS; HUMAN; IMMUNE DEFICIENCY; IMMUNOGLOBULIN DEFICIENCY; IMMUNOPHENOTYPING; LEUKOPENIA; LPS RESPONSIVE AND BEIGE LIKE ANCHOR GENE; LYMPHADENOPATHY; LYMPHOPROLIFERATIVE DISEASE; MAJOR CLINICAL STUDY; MITOCHONDRION; PANCYTOPENIA; PRIORITY JOURNAL; SPLENOMEGALY; T LYMPHOCYTE; WESTERN BLOTTING; CHILD; DNA SEQUENCE; GENETICS; INFANT; MALE; MUTATION; PRESCHOOL CHILD;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; APOPTOSIS; AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME; CHILD; CHILD, PRESCHOOL; HUMANS; INFANT; MALE; MUTATION; SEQUENCE ANALYSIS, DNA;

EID: 84929587365     PISSN: 15216616     EISSN: 15217035     Source Type: Journal    
DOI: 10.1016/j.clim.2015.04.007     Document Type: Article

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