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Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case report
Goh, Liuh Ling, Lee, Yingshan, Tan, Ee Shien, Lim, James Soon Chuan, Lim, Chia Wei, Dalan, RinkooVolume:
11
Language:
english
Journal:
BMC Medical Genomics
DOI:
10.1186/s12920-018-0356-8
Date:
December, 2018
File:
PDF, 1.07 MB
english, 2018