A novel frameshift variant of LMX1A that leads to autosomal dominant non-syndromic sensorineural hearing loss: functional characterization of the C-terminal domain in LMX1A.

Autor: Xiao, Min, Zheng, Yan, Huang, Kuo-Hsiang, Yu, Shanhe, Zhang, Wenbi, Xi, Yanping, Dou, Yan, Sun, Xiaoxi, Lei, Caixia, Yu, Huiqian
Zdroj: Human Molecular Genetics; 4/15/2023, Vol. 32 Issue 8, p1348-1360, 13p
Databáze: Complementary Index