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Uncovering potential single nucleotide polymorphisms, copy number variations and related signaling pathways in primary Sjogren’s syndrome

Primary Sjogren’s syndrome (pSS) is a complex systemic autoimmune disease, which is difficult to accurately diagnose due to symptom diversity in patients, especially at earlier stages. We tried to find potential single nucleotide polymorphisms (SNPs), copy number variations (CNVs) and related signal...

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Detalles Bibliográficos
Autores principales:	Qi, Xuan, Wang, Xi-Qin, Jin, Lu, Gao, Li-Xia, Guo, Hui-Fang
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Taylor & Francis 2021
Materias:	Research Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809958/ https://www.ncbi.nlm.nih.gov/pubmed/34723755 http://dx.doi.org/10.1080/21655979.2021.2000245

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