Whole-genome methylation analysis reveals novel epigenetic perturbations of congenital scoliosis

Congenital scoliosis (CS) is a congenital disease caused by malformations of vertebrae. Recent studies demonstrated that DNA modification could contribute to the pathogenesis of disease. This study aims to identify epigenetic perturbations that may contribute to the pathogenesis of CS. Four CS patie...

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Bibliografiske detaljer
Udgivet i:Mol Ther Nucleic Acids
Main Authors: Liu, Gang, Zhao, Hengqiang, Yan, Zihui, Zhao, Sen, Niu, Yuchen, Li, Xiaoxin, Wang, Shengru, Yang, Yang, Liu, Sen, Zhang, Terry Jianguo, Wu, Zhihong, Wu, Nan
Format: Artigo
Sprog:Inglês
Udgivet: American Society of Gene & Cell Therapy 2021
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Original Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7907230/
https://ncbi.nlm.nih.gov/pubmed/33717649
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.omtn.2021.02.002
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