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Oxidative Medicine and Cellular Longevity
Volume 2017, Article ID 9478946, 6 pages
https://doi.org/10.1155/2017/9478946
Research Article

Serum Bilirubin Levels and Promoter Variations in HMOX1 and UGT1A1 Genes in Patients with Fabry Disease

1Department of Medical Biochemistry and Laboratory Diagnostics, 1st Faculty of Medicine, Charles University, Katerinska 32, 12000 Prague 2, Czech Republic
22nd Department of Internal Medicine and Department of Cardiovascular Medicine, 1st Faculty of Medicine, Charles University, Katerinska 32, 12000 Prague 2, Czech Republic
34th Department of Internal Medicine, 1st Faculty of Medicine, Charles University, Katerinska 32, 12000 Prague 2, Czech Republic

Correspondence should be addressed to Libor Vítek; zc.tensec@ketiv

Received 22 May 2017; Accepted 9 July 2017; Published 16 August 2017

Academic Editor: Ryuichi Morishita

Copyright © 2017 Alena Jirásková 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

Alena Jirásková, Giulia Bortolussi, Gabriela Dostálová, et al., “Serum Bilirubin Levels and Promoter Variations in HMOX1 and UGT1A1 Genes in Patients with Fabry Disease,” Oxidative Medicine and Cellular Longevity, vol. 2017, Article ID 9478946, 6 pages, 2017. https://doi.org/10.1155/2017/9478946.