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

Analysis of <i>PTPN22</i> −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 <i>tyrosine phosphatase nonreceptor-type 22</i&...

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Main Authors: Paula Annahi Menchaca-Tapia, Miguel Marín-Rosales, Diana Celeste Salazar-Camarena, Alvaro Cruz, Edith Oregon-Romero, Raziel Tapia-Llanos, José Francisco Muñoz-Valle, Claudia Azucena Palafox-Sánchez
Format: Article
Language:English
Published: MDPI AG 2023-02-01
Series:Diagnostics
Subjects:
<i>PTPN22</i> polymorphisms
primary Sjögren’s Syndrome
<i>PTPN22</i> expression
Online Access:https://www.mdpi.com/2075-4418/13/5/899

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