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Prenatal and progressive coenzyme Q10 administration to mitigate muscle dysfunction in mitochondrial...

Prenatal and progressive coenzyme Q10 administration to mitigate muscle dysfunction in mitochondrial...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7c71afc86b444911a4efedc1c6edb74c

Prenatal and progressive coenzyme Q10 administration to mitigate muscle dysfunction in mitochondrial disease

About this item

Full title

Prenatal and progressive coenzyme Q10 administration to mitigate muscle dysfunction in mitochondrial disease

Publisher

Heidelberg: John Wiley & Sons, Inc

Journal title

Journal of Cachexia, Sarcopenia and Muscle, 2024-12, Vol.15 (6), p.2402-2416

Language

English

Formats

Publication information

Publisher

Heidelberg: John Wiley & Sons, Inc

More information

Scope and Contents

Contents

Background
ADCK genes encode aarF domain‐containing mitochondrial kinases involved in coenzyme Q (CoQ) biosynthesis and regulation. Haploinsufficiency of ADCK2 in humans leads to adult‐onset physical incapacity with reduced mitochondrial CoQ levels in skeletal muscle, resulting in mitochondrial myopathy and alterations in fatty acid β‐oxidation....

Alternative Titles

Full title

Prenatal and progressive coenzyme Q10 administration to mitigate muscle dysfunction in mitochondrial disease

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_7c71afc86b444911a4efedc1c6edb74c

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7c71afc86b444911a4efedc1c6edb74c

Other Identifiers

ISSN

2190-5991,2190-6009

E-ISSN

2190-6009

DOI

10.1002/jcsm.13574

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