3-mg-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

MainRecentTopDoctors

Spondylosis