Myotonia congenita with strabismus in a large family with a mutation in the SCN4A gene
Eye2012Vol. 26(8), pp. 1039–1043
Citations Over Time
Hongjun Du, Seanna Grob, Ling Zhao, Jong‐Dae Lee, Mahmoud El-Sahn, Guy Hughes, Jing Luo, K Schaf, Yaou Duan, J Quach, Xindong Wei, Peter X. Shaw, David B. Granet, K Zhang
Related Papers
- → Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotonia(2014)34 cited
- → Ocular motor function in relation to gross motor function in congenital and childhood myotonic dystrophy type 1(2010)22 cited
- → Mechanisms of cold sensitivity of paramyotonia congenita mutation R1448H and overlap syndrome mutation M1360V(2003)19 cited
- → A novel CLCN1 mutation (G1652A) causing a mild phenotype of thomsen disease(2010)5 cited
- → A new method for selective diagnosis of the functional status of small nerve fibers(1987)