Molecular Insights into the Electron Transfer Flavoprotein Dehydrogenase (ETFDH) Mutation Induced Mitochondrial Dysfunction
碩士 === 臺北醫學大學 === 醫學檢驗暨生物技術學系所 === 102 === Abstract Multiple acyl-CoA dehydrogenase deficiency (MADD), glutaric aciduria type II, is an autosomal recessive inherited disorder of fatty acid metabolism. In most cases MADD is caused by variations in one of two genes encoding electron transfer flavopro...
Main Authors: | , |
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Other Authors: | |
Format: | Others |
Language: | en_US |
Published: |
2014
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Online Access: | http://ndltd.ncl.edu.tw/handle/xy45kb |