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...

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Bibliographic Details
Main Authors: Suphannee Chokchaiwong, 張婷
Other Authors: Shu-Huei Kao
Format: Others
Language:en_US
Published: 2014
Online Access:http://ndltd.ncl.edu.tw/handle/xy45kb