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Mitochondrial fatty acid oxidation disorders associated with short-chain Enoyl-CoA Hydratase (ECHS1) deficiency

Sharpe, Alice J. and McKenzie, Matthew 2018, Mitochondrial fatty acid oxidation disorders associated with short-chain Enoyl-CoA Hydratase (ECHS1) deficiency, Cells, vol. 7, pp. 1-13, doi: 10.3390/cells7060046.

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Title Mitochondrial fatty acid oxidation disorders associated with short-chain Enoyl-CoA Hydratase (ECHS1) deficiency
Author(s) Sharpe, Alice J.
McKenzie, MatthewORCID iD for McKenzie, Matthew orcid.org/0000-0001-7508-1800
Journal name Cells
Volume number 7
Article ID 46
Start page 1
End page 13
Total pages 13
Publisher MDPI
Place of publication Basel, Switzerland
Publication date 2018-05-23
ISSN 2073-4409
Keyword(s) ECHS1 deficiency
OXPHOS
fatty acid oxidation
metabolism
mitochondrial disease
oxidative phosphorylation
short-chain enoyl-CoA hydratase
Science & Technology
Life Sciences & Biomedicine
Cell Biology
3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY
BETA-OXIDATION
LEIGH-SYNDROME
RESPIRATORY-CHAIN
VALINE METABOLISM
MUTATIONS
DEFECTS
PHOSPHORYLATION
BIOCHEMISTRY
DYSKINESIAS
Language eng
DOI 10.3390/cells7060046
HERDC Research category C1.1 Refereed article in a scholarly journal
ERA Research output type C Journal article
Copyright notice ©2018, The Authors
Free to Read? Yes
Use Rights Creative Commons Attribution licence
Persistent URL http://hdl.handle.net/10536/DRO/DU:30111620

Document type: Journal Article
Collections: School of Life and Environmental Sciences
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Every reasonable effort has been made to ensure that permission has been obtained for items included in DRO. If you believe that your rights have been infringed by this repository, please contact drosupport@deakin.edu.au.