3‐Hydroxyisobutyrate dehydrogenase ( HIBADH ) deficiency—A novel disorder of valine metabolism-Reference-Cited by-同舟云学术

3‐Hydroxyisobutyrate dehydrogenase ( HIBADH ) deficiency—A novel disorder of valine metabolism

Published:2021-07-05 Issue:6 Volume:44 Page:1323-1329
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:Jrnl of Inher Metab Disea

Author:

Meyer Melanie¹,Hollenbeck Jana C.²,Reunert Janine¹,Seelhöfer Anja¹,Rust Stephan¹,Fobker Manfred³,Biskup Saskia⁴,Och Ulrike¹,Linden Mechthild⁵,Sass Jörn Oliver²,Marquardt Thorsten¹

Affiliation:

1. Department of General Pediatrics University Hospital Münster Germany

2. Bonn‐Rhein‐Sieg University of Applied Sciences Department of Natural Sciences & Institute for Functional Gene Analytics (IFGA), RG Inborn Errors of Metabolism Rheinbach Germany

3. Center for Laboratory Medicine University Hospital Münster Germany

4. CeGaT GmbH und Praxis für Humangenetik Tübingen Tübingen Germany

5. private address

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jimd.12410

Reference14 articles.

1. 3-Hydroxyisobutyric Aciduria: An Inborn Error of Valine Metabolism

2. 3-Hydroxyisobutyric Aciduria in Two Brothers