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  1. Use of a long-chain triglyceride-restricted/medium-chain triglyceride-supplemented diet...

    Malonyl coenzyme A (CoA) decarboxylase (EC 4.1.1.9, MCD) deficiency, or malonic aciduria, is a rare inborn error of metabolism characterised by a variable phenotype of developmental delay, seizures, cardiomyopathy and acidosis. There is no consensus

    http://iris.ucl.ac.uk/iris/publication/240686/2

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