Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy

出版年份 2017 全文链接

标题

作者

关键词

Genetics, Neuromuscular disease, Metabolic disease, Muscle disease

出版物

Volume 27, Issue 6, Pages 581-584

出版商

Elsevier BV

发表日期

2017-03-09

DOI

10.1016/j.nmd.2017.03.003

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