Clinical，pathological and gene mutation characteristics of 18 cases of riboflavinresponsive lipid storage myopathy caused by ETFDH gene mutation

QIAN Qi, CUI Wenhao, QU Qianqian, et al.

Journal of Apoplexy and Nervous Diseases ›› 2022, Vol. 39 ›› Issue (9) : 772-776.

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Journal of Apoplexy and Nervous Diseases ›› 2022, Vol. 39 ›› Issue (9) : 772-776. DOI: 10.19845/j.cnki.zfysjjbzz.2022.0194
J Apoplexy and Nervous Diseases

Clinical，pathological and gene mutation characteristics of 18 cases of riboflavinresponsive lipid storage myopathy caused by ETFDH gene mutation

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{{article.zuoZheEn_L}}. {{article.title_en}}[J]. {{journal.qiKanMingCheng_EN}}, 2022, 39(9): 772-776 https://doi.org/10.19845/j.cnki.zfysjjbzz.2022.0194

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