Genetic cause of immune dysregulation one gene or two?

Journal of Clinical Investigation

Volumn 126, Issue 11, 2016, Pages 4065-4067

  Tangye, Stuart G ^a,b  

^a GARVAN INSTITUTE OF MEDICAL RESEARCH   (Australia)

^b UNIVERSITY OF NEW SOUTH WALES   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOANTIBODY; ENDONUCLEASE; NEI ENDONUCLEASE VIII LIKE 3; TOLL LIKE RECEPTOR 3; UNCLASSIFIED DRUG; FLJ10858 PROTEIN, HUMAN; GLYCOSIDASE; TLR3 PROTEIN, HUMAN;

AUTOIMMUNITY; GENE IDENTIFICATION; GENE SEQUENCE; GENETIC TRAIT; HUMAN; IMMUNE DYSREGULATION; LOSS OF FUNCTION MUTATION; MONOGENIC DISORDER; NEPHRITIS; PHENOTYPE; PRIORITY JOURNAL; REGULATORY T LYMPHOCYTE; REVIEW; ANIMAL; AUTOIMMUNE DISEASE; FAMILY; FEMALE; GENETIC DISORDER; GENETIC PREDISPOSITION; GENETICS; IMMUNOLOGY; MALE; MUTATION;

ANIMALS; AUTOIMMUNE DISEASES; FAMILY; FEMALE; GENETIC DISEASES, INBORN; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MUTATION; N-GLYCOSYL HYDROLASES; TOLL-LIKE RECEPTOR 3;

EID: 84994573325     PISSN: 00219738     EISSN: 15588238     Source Type: Journal    
DOI: 10.1172/JCI90831     Document Type: Review

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