Genes, Vol. 12, Pages 1126: Novel FGFR1 Variants Are Associated with Congenital Scoliosis

In conclusion, FGFR1 variants identified in our patients led to only mild disruption to protein function, caused milder skeletal and cardiac phenotypes than those reported previously.

Source: Genes - July 24, 2021 Category: Genetics & Stem Cells 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 Tags: Article Source Type: research