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Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle

Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6208583

Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle

About this item

Full title

Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle

Publisher

New York: Springer US

Journal title

Reviews in endocrine & metabolic disorders, 2018-03, Vol.19 (1), p.93-106

Language

English

Formats

Publication information

Publisher

New York: Springer US

More information

Scope and Contents

Contents

Mitochondrial fatty acid oxidation is an essential pathway for energy production, especially during prolonged fasting and sub-maximal exercise. Long-chain fatty acids are the most abundant fatty acids in the human diet and in body stores, and more than 15 enzymes are involved in long-chain fatty acid oxidation. Pathogenic mutations in genes encodin...

Alternative Titles

Full title

Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6208583

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6208583

Other Identifiers

ISSN

1389-9155

E-ISSN

1573-2606

DOI

10.1007/s11154-018-9448-1

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