Arch Iran Med. 2017;
20(12): 767-769.
Abstract View: 2601
PDF Download: 1592
Letter to the Editor
Trifunctional Protein Deficiency Due to HADHB Mutations Is a Multisystem, β-Oxidation Disorder
Josef Finsterer
1*, Sinda Zarrouk-Mahjoub
21 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
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.