Table of Contents Author Guidelines Submit a Manuscript
Case Reports in Genetics
Volume 2015 (2015), Article ID 259627, 5 pages
http://dx.doi.org/10.1155/2015/259627
Case Report

Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect

1Division of Pediatric Genetics, Department of Pediatrics, Meram Medical Faculty, University of Necmettin Erbakan, Meram, 42080 Konya, Turkey
2Department of Medical Genetics, University of Pécs, Pécs, Hungary
3Szentagothai Research Centre, University of Pécs, Pécs, Hungary
4Division of Pediatric Cardiology, Department of Pediatrics, Meram Medical Faculty, University of Necmettin Erbakan, Meram, 42080 Konya, Turkey
5Tanyalcin Medical Laboratory, Selective Screening and Metabolism Unit, Izmir, Turkey

Received 19 February 2015; Revised 20 April 2015; Accepted 20 April 2015

Academic Editor: Patrick Morrison

Copyright © 2015 Hatice Mutlu-Albayrak et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Hatice Mutlu-Albayrak, Judit Bene, Mehmet Burhan Oflaz, Tijen Tanyalçın, Hüseyin Çaksen, and Bela Melegh, “Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect,” Case Reports in Genetics, vol. 2015, Article ID 259627, 5 pages, 2015. doi:10.1155/2015/259627