Inherent lipid metabolic dysfunction in glycogen storage disease IIIa.

Li, Xin-Hua; Gong, Qi-Ming; Ling, Yun; Huang, Chong; Yu, De-Min; Gu, Lei-Lei; Liao, Xiang-Wei; Zhang, Dong-Hua; Hu, Xi-Qi; Han, Yue; Kong, Xiao-Fei; Zhang, Xin-Xin

Li, Xin-Hua; Gong, Qi-Ming; Ling, Yun; Huang, Chong; Yu, De-Min; Gu, Lei-Lei; Liao, Xiang-Wei; Zhang, Dong-Hua; Hu, Xi-Qi; Han, Yue; Kong, Xiao-Fei; Zhang, Xin-Xin.

Biochem Biophys Res Commun ; 455(1-2): 90-7, 2014 Dec 05.

Article in En | MEDLINE | ID: mdl-25451272

Subject(s)

Glycogen Debranching Enzyme System/genetics; Glycogen Storage Disease Type III/genetics; Mutation; Acyl-CoA Dehydrogenase/deficiency; Adolescent; Cells, Cultured; Fatty Acids/biosynthesis; Fatty Acids, Unsaturated/biosynthesis; Gene Expression; Glycogen Storage Disease Type III/diagnosis; Glycogen Storage Disease Type III/metabolism; Humans; Lipid Metabolism, Inborn Errors/diagnosis; Male

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Database: MEDLINE Main subject: Glycogen Debranching Enzyme System / Glycogen Storage Disease Type III / Mutation Type of study: Diagnostic_studies Limits: Adolescent / Humans / Male Language: En Journal: Biochem Biophys Res Commun Year: 2014 Type: Article

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