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    Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: urinary organic acid profiles and expanded spectrum of mutations by Pitt, James J. (Author) , Peters, Heidi (Author) , Boneh, Avihu (Author) , Yaplito‐Lee, Joy (Author) , Wieser, Stefanie (Author) , Hinderhofer, Katrin (Author) , Johnson, David (Author) , Zschocke, Johannes (Author) ,


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