| First Author | Grompe M | Year | 1992 |
| Journal | Biochem Med Metab Biol | Volume | 48 |
| Issue | 1 | Pages | 26-31 |
| PubMed ID | 1524868 | Mgi Jnum | J:2852 |
| Mgi Id | MGI:51372 | Doi | 10.1016/0885-4505(92)90044-y |
| Citation | Grompe M, et al. (1992) Nucleotide sequence of a cDNA encoding murine fumarylacetoacetate hydrolase. Biochem Med Metab Biol 48(1):26-31 |
| abstractText | Hereditary tyrosinemia type I is caused by deficiency of the enzyme fumarylacetoacetate hydrolase (FAH) (EC 3.7.1.2), the final step in tyrosine degradation. We report here the cloning and sequencing of a full length cDNA coding for murine FAH. This cDNA is highly homologous to the previously cloned human and rat genes. |
