Motor neuron disease gene sequencing
收藏NIAID Data Ecosystem2026-03-11 收录
下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA601896
下载链接
链接失效反馈官方服务：
资源简介：
We reported a rare congenital nemaline myopathy caused by a new nebulin (NEB) mutation in adult onset with weakness of the distal end of the lower limb for the first time which was comfirmed by next generation sequencing.
创建时间：
2020-01-17
