Both ETFDH mutations and FAD...

Annals of Neurology 2018 / 09

Both ETFDH mutations and FAD homeostasis disturbance are essential for developing riboflavin-responsive multiple Acyl-CoA dehydrogenation deficiency

Xu, Jingwen, Li, Duoling, Lv, Jingwei, Xu, Xuebi, Wen, Bing, Lin, Pengfei, Liu, Fuchen, Ji, Kunqian, Shan, Jingli, Li, Honghao, Li, Wei, Zhao, Yuying, Zhao, Dandan, Pok, Joo Y., Yan, Chuanzhu
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Language:
english
Journal:
Annals of Neurology
DOI:
10.1002/ana.25338
Date:
September, 2018
File:
PDF, 1.72 MB
english, 2018
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