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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 D...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2487435733

Insights from Animal Models on the Pathophysiology of Hyperphenylalaninemia: Role of Mitochondrial Dysfunction, Oxidative Stress and Inflammation

About this item

Full title

Insights from Animal Models on the Pathophysiology of Hyperphenylalaninemia: Role of Mitochondrial Dysfunction, Oxidative Stress and Inflammation

Publisher

New York: Springer US

Journal title

Molecular neurobiology, 2021-06, Vol.58 (6), p.2897-2909

Language

English

Formats

Publication information

Publisher

New York: Springer US

More information

Scope and Contents

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...

Alternative Titles

Full title

Insights from Animal Models on the Pathophysiology of Hyperphenylalaninemia: Role of Mitochondrial Dysfunction, Oxidative Stress and Inflammation

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2487435733

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2487435733

Other Identifiers

ISSN

0893-7648

E-ISSN

1559-1182

DOI

10.1007/s12035-021-02304-1

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