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

Author:

Grünert Sarah C.,Foster William,Schumann Anke,Lund Allan,Pontes Christina,Roloff Sylvia,Weinhold Natalie,Yue Wyatt W.,AlAsmari Ali,Obaid Osama A.,Faqeih Eissa Ali,Stübbe Lisa,Yamamoto Raina,Gemperle-Britschgi Corinne,Walter Melanie,Spiekerkoetter Ute,Mackinnon Sabrina,Sass Jörn OliverORCID

Publisher

Elsevier BV

Subject

General Medicine,Biochemistry

Reference34 articles.

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2. Inborn errors of ketone body metabolism and transport: an update for the clinic and for clinical laboratories;Sass;J. Inborn Errors Metab. Screen.,2018

3. Sass JO, Grünert SC. Disorders of ketone body metabolism. In: Blau N, Dionisi-Vici C, Ferreira C, Vianey-Saban C, van Karnebeek C, editors. Physician’s Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases. second ed.. Springer; in press.

4. Inborn errors of ketogenesis and ketone body utilization;Sass;J. Inherit. Metab. Dis.,2012

5. A new syndrome of ketoacidosis in infancy;Cornblath;J. Pediatr.,1971

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