3 methylglutaconyl coa hydratase deficiency

Methylglutaconyl-CoA hydratase, mitochondrial (339 aa, ~36 kDa) is encoded by the human AUH gene. This protein is involved in amino acid catabolism.

Disease Alternative Name

methylglutaconyl-coa hydratase
mitochondrial
mga type i
au rna-binding protein/enoyl-coenzyme a hydratase
au-specific rna-binding protein/enoyl-coa hydratase
au rna-binding protein
au-binding protein/enoyl-coa hydratase
au-specific rna binding protein
3-methylglutaconyl-coa hydratase
au rna binding protein
ec 4.2.1.18
auh
enoyl-coenzyme a hydratase
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