Multiple Acyl-CoA Dehydrogenation Deficiency (Glutaric Aciduria Type II) with a Novel Mutation of Electron Transfer Flavoprotein-Dehydrogenase in a Cat

Multiple acyl-CoA dehydrogenation deficiency (MADD; also known as glutaric aciduria type II) is a human autosomal recessive disease classified as one of the mitochondrial fatty-acid oxidation disorders. MADD is caused by a defect in the electron transfer flavoprotein (ETF) or ETF dehydrogenase (ETFD...

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Main Authors: Wakitani, Shoichi, Torisu, Shidow, Yoshino, Taiki, Hattanda, Kazuhisa, Yamato, Osamu, Tasaki, Ryuji, Fujita, Haruo, Nishino, Koichiro
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4110340/
https://ncbi.nlm.nih.gov/pubmed/24142280
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2013_268
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