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Enzyme Research
Volume 2016, Article ID 9040616, 7 pages
Research Article

Molecular Analysis of CYP21A2 Gene Mutations among Iraqi Patients with Congenital Adrenal Hyperplasia

1Genetic Counseling Clinic and Genetics Laboratory, The Teaching Laboratories, Medical City, Baghdad, Iraq
2Department of Pathology, College of Medicine, Baghdad University, Baghdad, Iraq
3Department of Pediatrics, College of Medicine, Baghdad University and Pediatric Endocrine Consultation Clinic, Children Welfare Hospital, Baghdad, Iraq
4ViennaLab Diagnostics GmbH, Gaudenzdorfer Guertel 43-45, 1120 Vienna, Austria
5National Center of Hematology, Al-Mustansiriya University, Baghdad, Iraq

Received 12 June 2016; Accepted 31 August 2016

Academic Editor: Hartmut Kuhn

Copyright © 2016 Ruqayah G. Y. Al-Obaidi 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.

Citations to this Article [1 citation]

The following is the list of published articles that have cited the current article.

  • Bo Zhang, Lin Lu, and Zhaolin Lu, “Molecular diagnosis of Chinese patients with 21-hydroxylase deficiency and analysis of genotype–phenotype correlations,” Journal of International Medical Research, pp. 030006051668520, 2017. View at Publisher · View at Google Scholar