https://pmc.ncbi.nlm.nih.gov/articles/PMC22879/
Deficient DNA-ligase activity in the metabolic disease tyrosinemia type I - PMC
Hereditary tyrosinemia type I (HT1) is an autosomal recessive inborn error of metabolism caused by the deficiency of fumarylacetoacetate hydrolase, the last...
tyrosinemia type idna ligase