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This was confirmed by the detection of a mutation within <jats:italic>GLUT2<\/jats:italic>, the gene encoding the liver\u2010type facilitative glucose transporter. The study of the respiratory chain revealed a deficiency of complexes I, III and IV in muscle. Mechanisms responsible for an impairment of mitochondrial function, which we interpret as a secondary phenomenon, are discussed.<\/jats:p>","DOI":"10.1023\/a:1020147716990","type":"journal-article","created":{"date-parts":[[2003,3,15]],"date-time":"2003-03-15T13:36:10Z","timestamp":1047735370000},"page":"379-384","source":"Crossref","is-referenced-by-count":20,"title":["A secondary respiratory chain defect in a patient with Fanconi\u2013Bickel syndrome"],"prefix":"10.1002","volume":"25","author":[{"given":"M. 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