Your search returned products across suppliers with conjugation options.

This gene encodes the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia (HT). [provided by RefSeq, Jul 2008]
 

Verification

Prior to displaying your results, please confirm you are a real person.

By continuing, you agree to the FluoroFinder Terms and Conditions.

Selected products
Remove all from compare list