Mitochondrial fatty acid oxidation disorders associated with short-chain enoyl-CoA hydratase (ECHS1) deficiency
Version 3 2024-06-18, 09:30
Version 2 2024-06-05, 00:13
Version 1 2018-05-23, 00:00
journal contribution
posted on 2024-06-18, 09:30 authored by AJ Sharpe, Matthew McKenzieMatthew McKenzieMitochondrial fatty acid oxidation disorders associated with short-chain enoyl-CoA hydratase (ECHS1) deficiency
History
Related Materials
- 1.
Location
SwitzerlandOpen access
- Yes
Link to full text
Language
EnglishPublication classification
C Journal article, C1.1 Refereed article in a scholarly journalCopyright notice
2018, The AuthorsJournal
CellsVolume
7Article number
ARTN 46Pagination
1 - 13ISSN
2073-4409eISSN
2073-4409Issue
6Publisher
MDPIUsage metrics
Keywords
Science & TechnologyLife Sciences & BiomedicineCell Biologymitochondrial diseasefatty acid oxidationshort-chain enoyl-CoA hydrataseECHS1 deficiencymetabolismoxidative phosphorylationOXPHOSBETA-OXIDATIONLEIGH-SYNDROMEDEHYDROGENASE-DEFICIENCYMUTATIONSMETABOLISMDEFECTSBIOCHEMISTRYPATIENTLIVERSchool of Life and Environmental Sciences3101 Biochemistry and cell biology
Licence
Exports
RefWorks
BibTeX
Ref. manager
Endnote
DataCite
NLM
DC