دورية أكاديمية

Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature review

التفاصيل البيبلوغرافية
العنوان: Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature review
المؤلفون: 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
المصدر: In Seizure: European Journal of Epilepsy April 2018 57:80-86
قاعدة البيانات: ScienceDirect
الوصف
تدمد:10591311
DOI:10.1016/j.seizure.2018.03.015