Now showing items 1-1 of 1
Determining DNA damage and repair in human cells exposed to metabolites characteristic for tyrosinemia
(North-West University, 2005)
Hereditary Tyrosinemia (HTI) is an autosomal recessive disorder caused by a deficiency of fumarylacetoacetate hydrolase (FAH) but the mechanism by which the hepatic and renal symptoms of HTI arise is largely unknown. The ...