Formation of 3‐hydroxyglutaric acid in glutaric aciduria type I: in vitro participation of medium chain acyl‐CoA dehydrogenase-Reference-Cited by-同舟云学术

Formation of 3‐hydroxyglutaric acid in glutaric aciduria type I: in vitro participation of medium chain acyl‐CoA dehydrogenase

Published:2019-03-26 Issue:1 Volume:47 Page:30-34
ISSN:2192-8312
Container-title:JIMD Reports
language:en
Short-container-title:JIMD Reports

Author:

Peters Verena¹^ORCID,Morath Marina¹,Mack Matthias²,Liesert Michael³,Buckel Wolfgang³,Hoffmann Georg F.¹,Vockley Jerry⁴,Ghisla Sandro⁵,Zschocke Johannes⁶^ORCID

Affiliation:

1. Center für Paediatric and Adolescent Medicine University of Heidelberg Germany

2. Institut für Technische Mikrobiologie Hochschule Mannheim Germany

3. Laboratorium für Mikrobiologie, Fachbereich Biologie Philipps‐Universität Marburg Germany

4. Department of Pediatric and Human Genetics Children's Hospital of Pittsburgh and University of Pittsburgh Pittsburgh Pennsylvania

5. Department of Biology, Section of Natural Sciences Universität Konstanz Germany

6. Division of Human Genetics Medical University Innsbruck Austria

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Biochemistry, Genetics and Molecular Biology (miscellaneous),Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jmd2.12026

Reference20 articles.

1. Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision

2. Glutaric acidemia type 1

3. Glutaric aciduria; A “new” disorder of amino acid metabolism

4. Glutaric aciduria type I: From clinical, biochemical and molecular diversity to successful therapy

5. Glutaryl-CoA Dehydrogenase Deficiency in Spain: Evidence of Two Groups of Patients, Genetically, and Biochemically Distinct

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