Chronic Phenotype Characterization of a Large-Animal Model of Hereditary Tyrosinemia Type 1

Hereditary tyrosinemia type 1 (HT1) is an autosomal recessive disease caused by deficiency in fumarylacetoacetate hydrolase, the last enzyme in the tyrosine catabolic pathway. In this study, we investigated whether fumarylacetoacetate hydrolase deficient (FAH(−/−)) pigs, a novel large-animal model o...

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Publicat a:Am J Pathol
Autors principals: Elgilani, Faysal, Mao, Shennen A., Glorioso, Jaime M., Yin, Meng, Iankov, Ianko D., Singh, Anisha, Amiot, Bruce, Rinaldo, Piero, Marler, Ronald J., Ehman, Richard L., Grompe, Markus, Lillegard, Joseph B., Hickey, Raymond D., Nyberg, Scott L.
Format: Artigo
Idioma:Inglês
Publicat: American Society for Investigative Pathology 2017
Matèries:
Regular Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5225308/
https://ncbi.nlm.nih.gov/pubmed/27855279
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajpath.2016.09.013
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