Fumarylacetoacetate hydrolase deficient pigs are a novel large animal model of metabolic liver disease

Hereditary tyrosinemia type I (HT1) is caused by deficiency in fumarylacetoacetate hydrolase (FAH), an enzyme that catalyzes the last step of tyrosine metabolism. The most severe form of the disease presents acutely during infancy, and is characterized by severe liver involvement, most commonly resu...

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Bibliografiset tiedot
Päätekijät: Hickey, Raymond D., Mao, Shennen A., Glorioso, Jaime, Lillegard, Joseph B., Fisher, James E., Amiot, Bruce, Rinaldo, Piero, Harding, Cary O., Marler, Ronald, Finegold, Milton J., Grompe, Markus, Nyberg, Scott L.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2014
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4096906/
https://ncbi.nlm.nih.gov/pubmed/24879068
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.scr.2014.05.003
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