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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FAHBA-20-REGO | 20 (40 μL) | 200 μL |
|
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| FAHBA-20-REGR | 20 (40 μL) | 200 μL |
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| FAHBA-20-ORGR | 20 (40 μL) | 200 μL |
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| FAHBA-20-GOGR | 20 (40 μL) | 200 μL |
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| FAHBA-20-GRRE | 20 (40 μL) | 200 μL |
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| FAHBA-20-GROR | 20 (40 μL) | 200 μL |
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| FAHBA-20-GRGO | 20 (40 μL) | 200 μL |
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| FAHBA-20-AQOR | 20 (40 μL) | 200 μL |
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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]
Gene Symbol : FAH
Gene Name : Fumarylacetoacetate hydrolase
Chromosome : CHR 15: 801,528,90-801,865,81
Locus : 15q25.1
Alt. Genes : KIF20A
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