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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
Sarar Mohamed
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.
MD, FRCPCHSuzan El-Kholy
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.
MDNasir Al-Juryyan
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.
MDAbdulrahman M. Al-Nemri
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.
MDKhaled K. Abu-Amero
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.
PhD, FRCPathReferences
- ↵
- Speiser PW,
- Azziz R,
- Baskin LS,
- Ghizzoni L,
- Hensle TW,
- Merke DP,
- et al.
- ↵
- White PC
- ↵(2012) Ministry of Health. National Newborn Screening Program. Saudi Arabia. Available from: [email protected]. Accessed 2014 November 14.
- ↵
- Toraman B,
- Ökten A,
- Kalay E,
- Karagüzel G,
- Dinçer T,
- Açıkgöz EG,
- et al.
- ↵
- ↵
- ↵
- Finkielstain GP,
- Chen W,
- Mehta SP,
- Fujimura FK,
- Hanna RM,
- Van Ryzin C,
- et al.
- ↵
- Bizzarri C,
- Crea F,
- Marini R,
- Benevento D,
- Porzio O,
- Ravà L,
- et al.
- ↵(2012) The 1000 Genomes Project Consortium. An integrated map of genetic variation from 1,092 human genomes. Nature 491:56–65.
- ↵The Human Gene Mutation Database, Institute of Medical Genetics in Cardiff. Available from: http://www.hgmd.org. Accessed 2014 November 14.
- ↵
In this issue
A CYP21A2 gene mutation in patients with congenital adrenal hyperplasia
Sarar Mohamed, Suzan El-Kholy, Nasir Al-Juryyan, Abdulrahman M. Al-Nemri, Khaled K. Abu-Amero
Saudi Medical Journal Jan 2015, 36 (1) 113-116; DOI: 10.15537/smj.2015.1.9697
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