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:	Xuan Qi, Xi-Qin Wang, Lu Jin, Li-Xia Gao, Hui-Fang Guo
Formato:	article
Lenguaje:	EN
Publicado:	Taylor & Francis Group 2021
Materias:	primary sjogren’s syndrome whole-exome sequencing single nucleotide variants copy number variations signaling pathway sanger sequencing in vitro validation Biotechnology TP248.13-248.65
Acceso en línea:	https://doaj.org/article/49f9848ab32445fa92d93c0edaac7568
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Uncovering potential single nucleotide polymorphisms, copy number variations and related signaling pathways in primary Sjogren’s syndrome

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