Trifunctional Protein Deficiency Due to HADHB Mutations Is a Multisystem, β-Oxidation Disorder

Josef Finsterer; Sinda Zarrouk-Mahjoub

Arch Iran Med. 2017;20(12): 767-769.

PMID: 29664318
Scopus ID: 85044254555

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Letter to the Editor

Trifunctional Protein Deficiency Due to HADHB Mutations Is a Multisystem, β-Oxidation Disorder

Josef Finsterer ¹^*, Sinda Zarrouk-Mahjoub ²

¹ Krankenanstalt Rudolfstiftung, Vienna, Austria
² University of Tunis El Manar and Genomics Platform, Pasteur Institute of Tunis, Tunisia

*Corresponding Author: Corresponding Author: Josef Finsterer, MD, PhD; Krankenanstalt Rudolfstiftung, Vienna, Austria, Postfach 20, 1180 Vienna, Austria, Europe. Tel: +43-1-7116592085, Fax: +43-1-4781711, Email: fifigs1@yahoo.de

Keywords: 1

Cite this article as: Finsterer J, Zarrouk-Mahjoub S. Trifunctional protein deficiency due to HADHB mutations is a multisystem, β-oxidation disorder. Arch Iran Med. 2017;20(12):767–769.

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