Autoimmunity in primary antibody deficiency is associated with protein tyrosine phosphatase nonreceptor type 22 (PTPN22)

Journal of Allergy and Clinical Immunology

Volumn 131, Issue 4, 2013, Pages

  Chew, Gary Y J ^a,b   Sinha, Umang ^a,b   Gatenby, Paul A ^a   Demalmanche, Theo ^c   Adelstein, Stephen ^d   Garsia, Roger ^d   Hissaria, Pravin ^e   French, Martyn A ^f   Wilson, Anastasia ^a,b   Whittle, Belinda ^b   Kirkpatrick, Philippa ^g   Riminton, D Sean ^g   Fulcher, David A ^h   Cook, Matthew C ^a,b  

^a CANBERRA HOSPITAL   (Australia)

^b Biology and Environment   (Australia)

^c HAPS Pathology   (Australia)

^d ROYAL PRINCE ALFRED HOSPITAL   (Australia)

^e ROYAL ADELAIDE HOSPITAL   (Australia)

^f UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^g Department of Microbiology and Infectious Diseases   (Australia)

^h WESTMEAD HOSPITAL   (Australia)

Author keywords

autoimmunity; common variable immunodeficiency; IgG subclass deficiency; Primary antibody deficiency; protein tyrosine phosphatase nonreceptor type 22; selective IgA deficiency; specific antibody deficiency

Indexed keywords

ARGININE; COMPLEMENT COMPONENT C3D RECEPTOR; GENOMIC DNA; IMMUNOGLOBULIN A; NON RECEPTOR PROTEIN TYROSINE PHOSPHATASE 22; TRYPTOPHAN;

ADOLESCENT; ADULT; AGED; ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; AUSTRALIA; AUTOIMMUNE DISEASE; B LYMPHOCYTE; CHILD; COHORT ANALYSIS; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC RISK; GENOTYPE; HUMAN; HUMORAL IMMUNE DEFICIENCY; IMMUNOGLOBULIN A DEFICIENCY; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRESCHOOL CHILD; PRIMARY ANTIBODY DEFICIENCY; PRIORITY JOURNAL; RISK ASSESSMENT; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84875719184     PISSN: 00916749     EISSN: 10976825     Source Type: Journal    
DOI: 10.1016/j.jaci.2012.06.023     Document Type: Article

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