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MOESM1 of Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations

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posted on 2019-12-19, 07:10 authored by Wei Chen, Youqiao Zhang, Yifeng Ni, Shaoyu Cai, Xin Zheng, Frank Mastaglia, Jingshan Wu
Additional file 1: Table S1. 381 cases of MADD with confirmed ETFDH mutation in the literature from Pubmed and Wanfang database.

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    BMC Neurology

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    Late-onset multiple acyl-CoA dehydrogenase deficiencyLipid storage myopathyETFDH geneC.250G > A mutationSouthern min populationEpidemiology

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