Succinyl-CoA:3-oxoacid coenzyme A transferase (SCOT) deficiency: A rare and potentially fatal metabolic disease
Document Type: | Article |
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Language: | English |
Author: | Sarah C. Grünert, William Foster, Anke Schumann, Allan Lund, Christina Pontes, Sylvia Roloff, Natalie Weinhold, Wyatt W. Yue, Ali AlAsmari, Osama A. Obaid, Eissa Ali Faqeih, Lisa Stübbe, Raina Yamamoto, Corinne Gemperle-Britschgi, Melanie Walter, Ute Spiekerkötter, Sabrina Mackinnon, Jörn Oliver Sass |
Parent Title (English): | Biochimie |
Volume: | 183 |
Issue: | April 2021 |
First Page: | 55 |
Last Page: | 62 |
ISSN: | 0300-9084 |
DOI: | https://doi.org/10.1016/j.biochi.2021.02.003 |
PMID: | https://pubmed.ncbi.nlm.nih.gov/33596448 |
Publisher: | Elsevier |
Place of publication: | Paris |
Date of first publication: | 2021/02/14 |
Funding Information: | JOS gratefully acknowledges financial support by the program 'FH Zeit fur Forschung' (project 'KETOplus', 005-1703-0016) of the Ministry of Culture and Science of the German State of North RhineWestphalia. |
Keyword: | Inborn error of metabolism; Ketoacidosis; Ketolysis; Ketone body utilization; Metabolic acidosis; OXCT1 |
Departments, institutes and facilities: | Fachbereich Angewandte Naturwissenschaften |
Institut für funktionale Gen-Analytik (IFGA) | |
Projects: | KETOplus - Ketonkörper: Mehr als nur Energieträger! (DE/MKW NRW/005-1703-0016) |
Dewey Decimal Classification (DDC): | 5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie |
Entry in this database: | 2021/03/02 |