Clinical review report Nitisinone (Nitisinone tablets) (Cycle pharmaceuticals ltd.)
Hereditary tyrosinemia type 1 (HT-1) is a rare, autosomal recessive disorder of amino acid metabolism. The deficiency of fumarylacetoacetate hydrolase (FAH), which is the last enzyme in the pathway of tyrosine catabolism, results in the accumulation of toxic metabolites in the FAH-deficient hepatocy...
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| Formato: | Libro electrónico |
| Idioma: | Inglés |
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Ottawa, Ontario :
Canadian Agency for Drugs and Technologies in Health
2018.
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| Ver en Biblioteca Universitat Ramon Llull: | https://discovery.url.edu/permalink/34CSUC_URL/1im36ta/alma991009820282406719 |
