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

• المؤلفون الرئيسيون: Gang Liu (مؤلف), Hengqiang Zhao (مؤلف), Zihui Yan (مؤلف), Sen Zhao (مؤلف), Yuchen Niu (مؤلف), Xiaoxin Li (مؤلف), Shengru Wang (مؤلف), Yang Yang (مؤلف), Sen Liu (مؤلف), Terry Jianguo Zhang (مؤلف), Zhihong Wu (مؤلف), Nan Wu (مؤلف)
• التنسيق: كتاب
• منشور في: Elsevier, 2021-03-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: Connect to this object online.

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...