All Relations between ivd and matrix compartment
Publication | Sentence | Publish Date | Extraction Date | Species |
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J Vockley, B Parimoo, K Tanak. Molecular characterization of four different classes of mutations in the isovaleryl-CoA dehydrogenase gene responsible for isovaleric acidemia. American journal of human genetics. vol 49. issue 1. 1991-08-02. PMID:2063866. | isovaleric acidemia (iva) is an inborn error of leucine metabolism and is caused by a genetically determined deficiency of isovaleryl-coa dehydrogenase (ivd), a mitochondrial matrix enzyme. | 1991-08-02 | 2023-08-11 | Not clear |