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

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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Enregistré dans:
Détails bibliographiques
Auteurs principaux: Xuan Qi, Xi-Qin Wang, Lu Jin, Li-Xia Gao, Hui-Fang Guo
Format: article
Langue:EN
Publié: Taylor & Francis Group 2021
Sujets:
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
Accès en ligne:https://doaj.org/article/49f9848ab32445fa92d93c0edaac7568
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https://doaj.org/article/49f9848ab32445fa92d93c0edaac7568

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