A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH gene.

Authors	Zhang-Ning Zhao, Meng-Xin Bao, Gao-Ting Ma, Xiao-Min Liu, Wen-Juan Xu, Zhong-Wen Sun, Huan Chen, Mei-Jia Zhu
Journal	CNS neuroscience & therapeutics (CNS Neurosci Ther) Vol. 18 Issue 11 Pg. 952-4 (Nov 2012) ISSN: 1755-5949 [Electronic] England
PMID	23106979 (Publication Type: Case Reports, Letter)
Chemical References	Electron-Transferring Flavoproteins Iron-Sulfur Proteins Oxidoreductases Acting on CH-NH Group Donors electron-transferring-flavoprotein dehydrogenase
Topics	Electron-Transferring Flavoproteins (genetics) Humans Iron-Sulfur Proteins (genetics) Male Middle Aged Multiple Acyl Coenzyme A Dehydrogenase Deficiency (diagnosis, genetics) Mutation (genetics) Oxidoreductases Acting on CH-NH Group Donors (genetics)

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