Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature
Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature
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DOI：
10.1016/j.seizure.2018.03.015
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发表时间：
2018
期刊：
影响因子：
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通讯作者：
Cao Li
中科院分区：
文献类型：
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作者：
Tian Wo Tu;Liu Xiao Li;Xu Yang Qi;Huang Xiao Jun;Zhou Hai Yan;Wang Ying;Tang Hui Dong;Chen Sheng Di;Luan Xing Hua;Cao Li
