Insights from Animal Models on the Pathophysiology of Hyperphenylalaninemia: Role of Mitochondrial D...
Insights from Animal Models on the Pathophysiology of Hyperphenylalaninemia: Role of Mitochondrial Dysfunction, Oxidative Stress and Inflammation
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New York: Springer US
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Language
English
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New York: Springer US
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Contents
Phenylketonuria (PKU) is an inborn error of metabolism caused by phenylalanine hydroxylase (PAH) deficiency and characterized by elevated plasma levels of phenylalanine (hyperphenylalaninemia-HPA). In severe cases, PKU patients present with neurological dysfunction and hepatic damage, but the underlying mechanisms are not fully elucidated. Other fo...
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Full title
Insights from Animal Models on the Pathophysiology of Hyperphenylalaninemia: Role of Mitochondrial Dysfunction, Oxidative Stress and Inflammation
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TN_cdi_proquest_miscellaneous_2487435733
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2487435733
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ISSN
0893-7648
E-ISSN
1559-1182
DOI
10.1007/s12035-021-02304-1