Study of ETFDH gene mutations in a family with riboflavin-responsive lipid storage myopathy

Journal of Apoplexy and Nervous Diseases ›› 2018, Vol. 35 ›› Issue (10) : 927-929.

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Journal of Apoplexy and Nervous Diseases ›› 2018, Vol. 35 ›› Issue (10) : 927-929.

Study of ETFDH gene mutations in a family with riboflavin-responsive lipid storage myopathy

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{{article.zuoZheEn_L}}. {{article.title_en}}[J]. {{journal.qiKanMingCheng_EN}}, 2018, 35(10): 927-929

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