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Multiple acyl-CoA-dehydrogenase deficiency (MADD)--a novel mutation of electron-transferring-flavoprotein dehydrogenase ETFDH.
Lämmer, A B; Rolinski, B; Ahting, U; Heuss, D.
Affiliation
  • Lämmer AB; Department of Neurology, University of Erlangen, Schwabachanlage 6, 91054 Erlangen, Germany. alexandra.laemmer@uk-erlangen.de
J Neurol Sci ; 307(1-2): 166-7, 2011 Aug 15.
Article in En | MEDLINE | ID: mdl-21616504
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mutation, Missense / Mitochondrial Diseases / Electron-Transferring Flavoproteins / Electron Transport / Multiple Acyl Coenzyme A Dehydrogenase Deficiency / Oxidoreductases Acting on CH-NH Group Donors / Iron-Sulfur Proteins Type of study: Diagnostic_studies Limits: Adult / Humans / Male Language: En Journal: J Neurol Sci Year: 2011 Document type: Article Affiliation country: Alemania Country of publication: Países Bajos
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mutation, Missense / Mitochondrial Diseases / Electron-Transferring Flavoproteins / Electron Transport / Multiple Acyl Coenzyme A Dehydrogenase Deficiency / Oxidoreductases Acting on CH-NH Group Donors / Iron-Sulfur Proteins Type of study: Diagnostic_studies Limits: Adult / Humans / Male Language: En Journal: J Neurol Sci Year: 2011 Document type: Article Affiliation country: Alemania Country of publication: Países Bajos