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3-methylglutaconic aciduria


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Any condition in which there is excess 3‐methylglutaconic acid in urine. Type I is due to deficiency of a specific hydratase that converts 3‐methylglutaconyl‐CoA to 3‐hydroxy‐3‐methylglutaryl‐CoA in mitochondria during catabolism ...

Subjects: Chemistry.


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