EHHADH explained

EHHADH is a human gene that encodes for a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. Mutations of the gene are a cause of peroxisomal disorders such as Zellweger syndrome. ^[1]

See also

• HSD17B4

Notes and References

1. Web site: EHHADH enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase [Homo sapiens (human) ]]. NCBI. 6 September 2017. 12 September 2017.