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Mitochondrial Genetic Disorders: Cell Signaling and Pharmacological Therapies

Mitochondrial Genetic Disorders: Cell Signaling and Pharmacological Therapies

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e6b03c80e8984c9f889a65cee65a32a9

Mitochondrial Genetic Disorders: Cell Signaling and Pharmacological Therapies

About this item

Full title

Mitochondrial Genetic Disorders: Cell Signaling and Pharmacological Therapies

Author / Creator

Publisher

Switzerland: MDPI AG

Journal title

Cells (Basel, Switzerland), 2019-03, Vol.8 (4), p.289

Language

English

Formats

Publication information

Publisher

Switzerland: MDPI AG

More information

Scope and Contents

Contents

Mitochondrial fatty acid oxidation (FAO) and respiratory chain (RC) defects form a large group of inherited monogenic disorders sharing many common clinical and pathophysiological features, including disruption of mitochondrial bioenergetics, but also, for example, oxidative stress and accumulation of noxious metabolites. Interestingly, several tra...

Alternative Titles

Full title

Mitochondrial Genetic Disorders: Cell Signaling and Pharmacological Therapies

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_e6b03c80e8984c9f889a65cee65a32a9

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e6b03c80e8984c9f889a65cee65a32a9

Other Identifiers

ISSN

2073-4409

E-ISSN

2073-4409

DOI

10.3390/cells8040289

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