A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis

American Journal of Human Genetics

Volumn 75, Issue 2, 2004, Pages 330-337

  Begovich, Ann B ^a   Carlton, Victoria E H ^a   Honigberg, Lee A ^a   Schrodi, Steven J ^a   Chokkalingam, Anand P ^a   Alexander, Heather C ^a   Ardlie, Kristin G ^b   Huang, Qiqing ^c   Smith, Ashley M ^a   Spoerke, Jill M ^a   Conn, Marion T ^a   Chang, Monica ^a   Chang, Sheng Yung P ^a   Saiki, Randall K ^a   Catanese, Joseph J ^a   Leong, Diane U ^a   Garcia, Veronica E ^a   McAllister, Linda B ^a   Jeffery, Douglas A ^a   Lee, Annette T ^d   Batliwalla, Franak ^d   Remmers, Elaine ^e   Criswell, Lindsey A ^f   Seldin, Michael F ^g   Kastner, Daniel L ^e   Amos, Christopher I ^c   Sninsky, John J ^a   Gregersen, Peter K ^d   more..

^a CELERA   (United States)

^b Genomics Collaborative   (United States)

^c UNIVERSITY OF TEXAS MD ANDERSON CANCER CENTER   (United States)

^d University of Texas ^*  (United States)

^e NATIONAL INSTITUTES OF HEALTH   (United States)

^f UNIVERSITY OF CALIFORNIA   (United States)

^g UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CSK PROTEIN; GENE PRODUCT; LYP PROTEIN; PROLINE; PROTEIN TYROSINE PHOSPHATASE; REGULATOR PROTEIN; UNCLASSIFIED DRUG;

ADULT; AGED; ALLELE; ARTICLE; AUTOIMMUNE DISEASE; CASE CONTROL STUDY; CAUCASIAN; CONTROLLED STUDY; DISEASE CARRIER; GENE; GENE IDENTIFICATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; HUMAN; IMMUNOREACTIVITY; INSULIN DEPENDENT DIABETES MELLITUS; MAJOR CLINICAL STUDY; MISSENSE MUTATION; P1 PROLINE RICH MOTIF; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN INTERACTION; PROTEIN MOTIF; PTPN22 GENE; RHEUMATOID ARTHRITIS; SINGLE NUCLEOTIDE POLYMORPHISM; T LYMPHOCYTE ACTIVATION;

EID: 3242713277     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/422827     Document Type: Article

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