Lack of association of the PTPN22 gene polymorphism R620W with systemic sclerosis

Clinical and Experimental Rheumatology

Volumn 24, Issue 3, 2006, Pages 321-324

  Balada, Eva ^a   Simeón Aznar, Carmen Pilar ^a   Serrano Acedo, Silvia ^a   Martínez Lostao, Luis ^a   Selva O'Callaghan, Albert ^a   Fonollosa Pla, Vicente ^a   Vilardell Tarrés, Miquel ^a  

^a HOSPITAL UNIVERSITARI VALL D HEBRON   (Spain)

Author keywords

PTPN22; SNP; Systemic sclerosis

Indexed keywords

CENTROMERE ANTIBODY; GENOMIC DNA; PROTEIN TYROSINE PHOSPHATASE; PROTEIN TYROSINE PHOSPHATASE N22; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; DNA ISOLATION; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC ASSOCIATION; GENOTYPE; HETEROZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; PATHOGENESIS; POLYMERASE CHAIN REACTION; PREVALENCE; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL SIGNIFICANCE; SYSTEMIC SCLEROSIS;

ANTIBODIES, ANTINUCLEAR; CENTROMERE; DNA TOPOISOMERASES, TYPE I; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN-TYROSINE-PHOSPHATASE; SCLERODERMA, SYSTEMIC;

EID: 33746591498     PISSN: 0392856X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (21)

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