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Arch Iran Med. 2017;20(12): 767-769.
PMID: 29664318
Scopus ID: 85044254555
  Abstract View: 1810
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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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Submitted: 14 Jun 2017
Accepted: 18 Oct 2017
ePublished: 01 Dec 2017
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