Browsing by Author "1847946b-0bd6-4689-9bc5-ae0ff6157039"
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Lagos García, María Ignacia; Parra, Alicia de la; Arias Pefaur, Carolina; Arredondo Olguín, Miguel Armando; Cabello Andrade, Juan (Elsevier, 2017)Introduction: Tyrosinemia Type 1 (HT1) is an autosomal recessive disorder caused by a defect in the enzyme fumarylacetoacetate hydroxylase in the tyrosine pathway. Implementation of nitisinone (NTBC) treatment has dramatically ...