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Article

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

Bioengineered - 1 Dec 2021

Qi Xuan, Wang Xi-Qin, Jin Lu, Gao Li-Xia, Guo Hui-Fang

Abstract excerpt

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 signaling pathways. Genomic DNA was extracted from peripheral blood of 12 individuals (7 individuals from 3 pSS pedigrees...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 34723755
DOI: 10.1080/21655979.2021.2000245
PMCID: PMC8809958

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