PTPN22 polymorphism is related to autoimmune disease risk in patients with turner syndrome

Scandinavian Journal of Immunology

Volumn 72, Issue 3, 2010, Pages 256-259

  Bianco, B ^a,b   Verreschi, I T N ^a   Oliveira, K C ^a   Guedes, A D ^a   Galera, B B ^c   Galera, M F ^c   Barbosa, C P ^b   Lipay, M V N ^a  

^a FEDERAL UNIVERSITY OF SÃO PAULO   (Brazil)

^b FACULDADE DE MEDICINA DO ABC   (Brazil)

^c UNIVERSITY OF CUIABÁ   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOIMMUNE DISEASE; AUTOIMMUNITY; BRAZIL; CONTROLLED STUDY; FEMALE; GENE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HIGH RISK PATIENT; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; PTPN22 GENE; REAL TIME POLYMERASE CHAIN REACTION; TURNER SYNDROME; ADOLESCENT; CHILD; CHROMOSOME ABERRATION; GENETICS; HETEROZYGOTE; HOMOZYGOTE; INFANT; MIDDLE AGED; PRESCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; YOUNG ADULT;

NON RECEPTOR PROTEIN TYROSINE PHOSPHATASE 22; PTPN22 PROTEIN, HUMAN;

ADOLESCENT; ADULT; AUTOIMMUNE DISEASES; BRAZIL; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; FEMALE; GENE FREQUENCY; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; INFANT; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN TYROSINE PHOSPHATASE, NON-RECEPTOR TYPE 22; TURNER SYNDROME; YOUNG ADULT;

EID: 77955302828     PISSN: 03009475     EISSN: 13653083     Source Type: Journal    
DOI: 10.1111/j.1365-3083.2010.02438.x     Document Type: Article

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