Novel <i>FGFR1</i> Variants Are Associated with Congenital Scoliosis

Novel <i>FGFR1</i> Variants Are Associated with Congenital Scoliosis

<i>FGFR1</i> encodes a transmembrane cytokine receptor, which is involved in the early development of the human embryo and plays an important role in gastrulation, organ specification and patterning of various tissues. Pathogenic <i>FGFR1</i> variants have been associated wit...

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Bibliographic Details
Main Authors: Shengru Wang, Xiran Chai, Zihui Yan, Sen Zhao, Yang Yang, Xiaoxin Li, Yuchen Niu, Guanfeng Lin, Zhe Su, Zhihong Wu, Terry Jianguo Zhang, Nan Wu
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Genes
Subjects:
<i>FGFR1</i> (Fibroblast growth factor receptor 1)
genetic variations
congenital scoliosis
Online Access:https://www.mdpi.com/2073-4425/12/8/1126

Internet

https://www.mdpi.com/2073-4425/12/8/1126

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