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Williams Yuen
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Utilization of Hematin in Tyrosinemia Type I
Tyrosinemia type I is a rare autosomal recessive disorder characterized by a deficiency of the enzyme fumarylacetoacetate hydrolase (FAH), leading to the accumulation of toxic metabolites such as succinylacetone and tyrosine. Without proper management, tyrosinemia type I can result in severe liver dysfunction, renal impairment, and neurological com... Read More»
: J Obes Metab 2024, 7:225
10.4172/jomb.1000225Abstract Peer-reviewed Full Article Peer-reviewed Article PDF Mobile Full Article
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