Your search for "FAH" returned 47
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]
(Mouse) 14085, (Human) 2184, (Rat) 29383
(Mouse) P35505, (Mouse) Q3TY87, (Mouse) Q9QW65, (Human) P16930, (Human) B2R9X1, (Human) D3DW95, (Human) Q53XA7, (Rat) P25093
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