Volltext-Downloads (blau) und Frontdoor-Views (grau)
The search result changed since you submitted your search request. Documents might be displayed in a different sort order.
  • search hit 2 of 584
Back to Result List

Succinyl-CoA:3-oxoacid coenzyme A transferase (SCOT) deficiency: A rare and potentially fatal metabolic disease

Export metadata

Additional Services

Search Google Scholar Check availability

Statistics

Show usage statistics
Metadaten
Document Type:Article
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: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