Correction: Early onset combined immunodeficiency and autoimmunity in patients with loss-of-function mutation in LAT [The Journal of Experimental Medicine, 213, 7, (2016) (1185-1199)] DOI:10.1084/jem.20151110;Early onset combined immunodeficiency and autoimmunity in patients with loss-of-function mutation in LAT

Journal of Experimental Medicine

Volumn 213, Issue 7, 2016, Pages 1185-1199

  Keller, Baerbel ^a   Zaidman, Irina ^b   Yousefi, O Sascha ^a   Hershkovitz, Dov ^c   Stein, Jerry ^d   Unger, Susanne ^a   Schachtrup, Kristina ^a   Sigvardsson, Mikael ^e   Kuperman, Amir A ^f,g   Shaag, Avraham ^h   Schamel, Wolfgang W ^a   Elpeleg, Orly ^h   Warnatz, Klaus ^a   Stepensky, Polina ^h  

^a UNIVERSITY OF FREIBURG   (Germany)

^b Rambam Health Care Campus   (Israel)

^c BIO SS Centre for Biological Signalling Studies ^*  (Israel)

^d SCHNEIDER CHILDREN S MEDICAL CENTER OF ISRAEL   (Israel)

^e LINKÖPING UNIVERSITY   (Sweden)

^f WESTERN GALILEE HOSPITAL   (Israel)

^g BAR ILAN UNIVERSITY   (Israel)

^h HEBREW UNIVERSITY OF JERUSALEM   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIVIRUS AGENT; CALCIUM ION; CD28 ANTIGEN; CD3 ANTIGEN; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; IMMUNOGLOBULIN G; LAT PROTEIN; LYSOSOME ASSOCIATED MEMBRANE PROTEIN 1; MITOGEN ACTIVATED PROTEIN KINASE; STEROID; LAT PROTEIN, HUMAN; MEMBRANE PROTEIN; SIGNAL TRANSDUCING ADAPTOR PROTEIN;

ALLOGENEIC STEM CELL TRANSPLANTATION; ARTICLE; AUTOIMMUNE DISEASE; AUTOIMMUNE HEMOLYTIC ANEMIA; AUTOIMMUNITY; CALCIUM TRANSPORT; CASE REPORT; COMBINED IMMUNODEFICIENCY; CYTOMEGALOVIRUS INFECTION; EXON; FEMALE; GAMMA DELTA T LYMPHOCYTE; HOMOZYGOSITY; HUMAN; INFANT; LOSS OF FUNCTION MUTATION; LYMPHADENOPATHY; LYMPHOCYTE ACTIVATION; MALE; NONHUMAN; PLASMAPHERESIS; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; SPLENECTOMY; SPLENOMEGALY; T LYMPHOCYTE; THROMBOCYTOPENIA; THROMBOTIC THROMBOCYTOPENIC PURPURA; CALCIUM SIGNALING; GENETICS; HOMOZYGOTE; IMMUNOLOGY; MUTATION; PATHOLOGY; SEVERE COMBINED IMMUNODEFICIENCY;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; AUTOIMMUNE DISEASES; CALCIUM SIGNALING; EXONS; FEMALE; HOMOZYGOTE; HUMANS; MALE; MEMBRANE PROTEINS; MUTATION; NF-KAPPA B; SEVERE COMBINED IMMUNODEFICIENCY;

EID: 84977628587     PISSN: 00221007     EISSN: 15409538     Source Type: Journal    
DOI: 10.1084/jem.2015111005242017c     Document Type: Erratum

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