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by Lei, ZX and Chen, WJ and Liang, JQ and Wang, YJ and Jin, L and Xu, C and Kang, XJ
MEDICINE, ISSN 0025-7974, 05/2019, Volume 98, Issue 20, p. e15448
Background: The single nucleotide polymorphism (SNP) rs2476601 of the protein tyrosine phosphatase, nonreceptor type 22 (PTPN22) gene has been presented to... 
ALLELE | rs2476601 | C1858T | meta-analysis | PROTEIN-TYROSINE PHOSPHATASES | SUSCEPTIBILITY LOCI | polymorphism | PTPN22 | VARIANT | MEDICINE, GENERAL & INTERNAL | DISEASES | CTLA4 | alopecia areata | STRESS | T-CELLS | GENOME-WIDE ASSOCIATION | Medical research | Alopecia | Baldness | Medicine, Experimental | Genetic aspects | Single nucleotide polymorphisms | Research | Risk factors
Journal Article
Journal Article
Journal Article
Inflammation Research, ISSN 1023-3830, 9/2017, Volume 66, Issue 9, pp. 775 - 781
Journal Article
Journal of Clinical Laboratory Analysis, ISSN 0887-8013, 03/2019, Volume 33, Issue 3, pp. e22710 - n/a
Journal Article
Journal Article
Journal Article
Molecular Genetics & Genomic Medicine, ISSN 2324-9269, 06/2019, Volume 7, Issue 6, pp. e661 - n/a
Background Susceptibility to Graves' disease (GD) is determined by various genetic factors; the gene encoding protein tyrosine phosphatase (PTPN22) may be one... 
Graves' disease | gene polymorphism | PTPN22 gene | RHEUMATOID-ARTHRITIS | C1858T | SINGLE-NUCLEOTIDE POLYMORPHISM | LYMPHOID TYROSINE PHOSPHATASE | VARIANT | LOCUS | GENE | AUTOIMMUNE THYROID-DISEASES | GENETICS & HEREDITY | METAANALYSIS REVEALS
Journal Article