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3-Methylcrotonylglycinuria 3-Methylcrotonylglycinuria is a disorder of leucine catabolism that results from defects in either of the two subunits of the biotin-requiring enzyme, 3-methylcrotonyl-CoA carboxylase (3MCC)

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Vials are vacuum sealed and stored in a temperature controlled, monitored cold storage system to preserve compound integrity throughout the supply chain

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