Reference Work Entry

Encyclopedia of Genetics, Genomics, Proteomics and Informatics

pp 1056-1056



Occurs in several human diseases when ketones accumulate due to a defect in succinyl-CoA, 3-ketoacid CoA-transferase, in diabetes mellitus, in Gierke’s disease (Type I glycogen storage disease), in glycinemia, in methylmalonic aciduria and in lactic aciduria. individual entries

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