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A CYP21A2 gene mutation in patients with congenital adrenal hyperplasia

Molecular genetics report from Saudi Arabia

Sarar Mohamed, Suzan El-Kholy, Nasir Al-Juryyan, Abdulrahman M. Al-Nemri and Khaled K. Abu-Amero
Saudi Medical Journal January 2015, 36 (1) 113-116; DOI: https://doi.org/10.15537/smj.2015.1.9697

Article Information

vol. 36 no. 1 113-116
DOI 
https://doi.org/10.15537/smj.2015.1.9697
PubMed 
25630015
Published By 
Saudi Medical Journal
Online ISSN 
1658-3175
History 
  • Received August 28, 2014
  • Accepted December 2, 2014
  • Published online January 1, 2015.
Copyright & Usage 
Copyright: © Saudi Medical Journal This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Author Information

  1. Sarar Mohamed, MD, FRCPCH⇑,
  2. Suzan El-Kholy, MD,
  3. Nasir Al-Juryyan, MD,
  4. Abdulrahman M. Al-Nemri, MD and
  5. Khaled K. Abu-Amero, PhD, FRCPath
  1. From the Department of Pediatrics (Mohamed, Al-Juryyan, Al-Nemri), the Department of Ophthalmology (Abu-Amero), College of Medicine, King Saud University, Riyadh, and the Department of Pediatrics (El-Kholy), King Fahad Military Complex, Dhahran, Kingdom of Saudi Arabia.
  1. Address correspondence and re-prints request to: Dr. Sarar Mohamed, Associate Professor, Department of Pediatrics, College of Medicine, King Saud University, PO Box 2925, Riyadh 11461, Kingdom of Saudi Arabia. Fax. +966 (11) 4672439. E-mail: sararmohamed{at}hotmail.com
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