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Genetic bases and clinical manifestations of coenzyme Q10 (CoQ10) deficiency

Genetic bases and clinical manifestations of coenzyme Q10 (CoQ10) deficiency

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1641858964

Genetic bases and clinical manifestations of coenzyme Q10 (CoQ10) deficiency

About this item

Full title

Genetic bases and clinical manifestations of coenzyme Q10 (CoQ10) deficiency

Publisher

Dordrecht: Springer Netherlands

Journal title

Journal of inherited metabolic disease, 2015-01, Vol.38 (1), p.145-156

Language

English

Formats

Publication information

Publisher

Dordrecht: Springer Netherlands

More information

Scope and Contents

Contents

Coenzyme Q
10
is a remarkable lipid involved in many cellular processes such as energy production through the mitochondrial respiratory chain (RC), beta-oxidation of fatty acids, and pyrimidine biosynthesis, but it is also one of the main cellular antioxidants. Its biosynthesis is still incompletely characterized and requires at least 15 gene...

Alternative Titles

Full title

Genetic bases and clinical manifestations of coenzyme Q10 (CoQ10) deficiency

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1641858964

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1641858964

Other Identifiers

ISSN

0141-8955

E-ISSN

1573-2665

DOI

10.1007/s10545-014-9749-9

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