Treatment of hereditary tyrosinaemia (fumarylacetoacetase deficiency) by enzyme substitution
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- Kvittingen, E. A., Halvorsen, S. and Jellum, E. Deficient fumarylacetoacetate fumarylhydrolase activity in lymphocytes and fibroblasts from patients with hereditary tyrosinaemia.Pediatr. Res. 14 (1983) 541–544Google Scholar
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