Tyrosinemia (TYRSN)
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-66816-1_1802-1
Reference10 articles.
1. Bliksrud YT, Brodtkorb E, Andresen PA, van den Berg IET, Kvittingen EA (2005) Tyrosinaemia type I–de novo mutation in liver tissue suppressing an inborn splicing defect. J Mol Med 83:406–410. https://doi.org/10.1007/s00109-005-0648-2
2. Chinsky JM et al (2017) Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations. Genet Med:19. https://doi.org/10.1038/gim.2017.101
3. Heylen E, Fau SG, Fau VM, Fau MS, Fau FJ, Nassogne MC (2012) Tyrosinemia type III detected via neonatal screening: management and outcome. Mol Genet Metab 107(3):605–607
4. Kvittingen EA, Halvorsen S, Jellum E (1983) Deficient fumarylacetoacetate fumarylhydrolase activity in lymphocytes and fibroblasts from patients with hereditary tyrosinemia. Pediatr Res 17:541–544. https://doi.org/10.1203/00006450-198307000-00005
5. Lindstedt S, Holme E, Lock EA, Hjalmarson O, Strandvik B (1992) Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase. Lancet 340:813–817. https://doi.org/10.1016/0140-6736(92)92685-9
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