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Analysis of PTPN22 −1123 G>C, +788 G>A and +1858 C>T Polymorphisms in Patients with Primary Sjögren’s Syndrome

Background: Primary Sjögren’s syndrome (pSS) is an autoimmune exocrinopathy characterized by lymphocytic infiltration, glandular dysfunction and systemic manifestations. Lyp protein is a negative regulator of the T cell receptor encoded by the tyrosine phosphatase nonreceptor-type 22 (PTPN22) gene....

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Detalles Bibliográficos
Autores principales:	Menchaca-Tapia, Paula Annahi, Marín-Rosales, Miguel, Salazar-Camarena, Diana Celeste, Cruz, Alvaro, Oregon-Romero, Edith, Tapia-Llanos, Raziel, Muñoz-Valle, José Francisco, Palafox-Sánchez, Claudia Azucena
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10001387/ https://www.ncbi.nlm.nih.gov/pubmed/36900045 http://dx.doi.org/10.3390/diagnostics13050899

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