期刊文献+
共找到1篇文章
< 1 >
每页显示 20 50 100
ovel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis 被引量:1
1
作者 yang-qi xu Xiao-Li Liu +3 位作者 Xiao-Jun Huang WO-Tu Tian Hui-Dong Tang Li Cao 《Chinese Medical Journal》 SCIE CAS CSCD 2018年第4期477-479,共3页
Myotonia congenita (MC) is a group of genetically and clinically heterogeneous congenital neuromuscular channelopathies, typically characterized by the delayed relaxation of the muscles after voluntary contraction, ... Myotonia congenita (MC) is a group of genetically and clinically heterogeneous congenital neuromuscular channelopathies, typically characterized by the delayed relaxation of the muscles after voluntary contraction, stifthess, hypertrophy, transient weakness, and cramping. 展开更多
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部