Motor neuron disease gene sequencing
收藏NIAID Data Ecosystem2026-05-01 收录
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https://www.ncbi.nlm.nih.gov/sra/SRP242530
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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：
2024-01-13
