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- W4254152005 abstract "Hereditary tyrosinemia type 1 (HT1), the most severe inborn error of the tyrosine degradation pathway, is due to a deficiency in fumarylacetoacetate hydrolase (FAH). The worldwide frequency of HT1 is" @default.
- W4254152005 created "2022-05-12" @default.
- W4254152005 date "2017-01-01" @default.
- W4254152005 modified "2023-10-18" @default.
- W4254152005 title "Hereditary Tyrosinemia" @default.
- W4254152005 doi "https://doi.org/10.1007/978-3-319-55780-9" @default.
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