A functional polymorphims (1858C/T) in the PTPN22 gene is linked and associated with type I diabetes in multiplex families

Genes and Immunity

Volumn 5, Issue 8, 2004, Pages 678-680

  Onengut Gumuscu, S ^a,b   Ewens, K G ^c   Spielman, R S ^c   Concannon, Patcon ^a,b  

^a BENAROYA RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Disease association; Functional SNP; Lymphoid specific phosphatase; Type I diabetes

Indexed keywords

CYSTEINE; PHOSPHATASE; PROTEIN PTPN22; THREONINE; UNCLASSIFIED DRUG; PROTEIN TYROSINE PHOSPHATASE; PROTEIN TYROSINE PHOSPHATASE LYP; PROTEIN-TYROSINE PHOSPHATASE LYP;

ALLELE; ARTICLE; CHROMOSOME 21; CHROMOSOME 3; CONTROLLED STUDY; GENE INTERACTION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC RISK; GENETIC VARIABILITY; GENOME ANALYSIS; GENOTYPE; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; MULTIGENE FAMILY; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; COMPARATIVE STUDY; GENETIC PREDISPOSITION; GENETICS; RISK FACTOR;

ALLELES; DIABETES MELLITUS, TYPE 1; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LINKAGE (GENETICS); POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN-TYROSINE-PHOSPHATASE; RISK FACTORS;

EID: 11044226181     PISSN: 14664879     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.gene.6364138     Document Type: Article

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