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dc.contributor.authorRakhimova M.B., Akhmedov Kh.S.-
dc.date.accessioned2024-12-16T19:13:21Z-
dc.date.available2024-12-16T19:13:21Z-
dc.date.issued2024-
dc.identifier.citationToshkenten_US
dc.identifier.issn2181-7812-
dc.identifier.urihttp://repo.tma.uz/xmlui/handle/1/367-
dc.description.abstractIn this review, we summarize the mechanism of how PTPN22 and its genetic variants are involved in the patho- physiology of autoimmune diseases. In addition, we sum up the findings of studies reporting the genetic association of PTPN22 with different types of diseases, including type 1 diabetes mellitus, systemic lupus erythematosus, juvenile idiopathic arthritis, and several other diseases. By understanding these findings comprehensively, we can explain the complex etiology of autoimmunity and help to determine the criteria of disease diagnosis and prognosis, as well as medication developments.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesUDC;616.72-002.772-
dc.subjectPTPN22, single nucleotide polymorphisms, autoimmune diseases, genetic association.en_US
dc.titleGenetic polymorphism of gene ptpn22 in autoimmune diseasesen_US
dc.typeArticleen_US
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