Journal of Obesity and Metabolism
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Clara Hildebrandt
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Genetic tyrosinemia type 1 (HT1) is a rare autosomal recessive disorder characterized by deficiency of the enzyme fumarylacetoacetate hydrolase (FAH), leading to the accumulation of toxic metabolites such as succinylacetone and tyrosine. This metabolic imbalance not only affects liver function but also impacts overall nutritional status, particular... Read More»
: J Obes Metab 2024, 7:220
10.4172/jomb.1000220Abstract Peer-reviewed Full Article Peer-reviewed Article PDF Mobile Full Article
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