Title of article
Trifunctional Protein Deficiency Due to HADHB Mutations Is a Multisystem, β-Oxidation Disorder
Author/Authors
Finsterer, Josef Krankenanstalt Rudolfstiftung - Vienna, Austria , Zarrouk-Mahjoub, Sinda University of Tunis El Manar and Genomics Platform - Pasteur Institute of Tunis, Tunisia
Pages
3
From page
767
To page
769
Abstract
With interest, we read the article by Shahrokhi et al about a new-born with a β-oxidation defect due to a mutation in the HADHB gene encoding the β-subunit of the trifunctional protein.1 We have the following comments and concerns.
Keywords
β-Oxidation , HADHB , Multisystem , Trifunctional
Journal title
Astroparticle Physics
Serial Year
2017
Record number
2446057
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