A CYP21A2 gene mutation in patients with congenital adrenal hyperplasia: Molecular genetics report from Saudi Arabia

OBJECTIVES: The aim of this study is to determine congenital adrenal hyperplasia (CAH) with the pattern of CYP21A2 gene-mutations in Saudi children. METHODS: Between January 2011 and March 2014 at King Fahad Military Complex, Dhahran, Saudi Arabia, we thoroughly examined 11 patients with CAH and 2 a...

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Detalles Bibliográficos
Autores principales: Mohamed, Sarar, El-Kholy, Suzan, Al-Juryyan, Nasir, Al-Nemri, Abdulrahman M., Abu-Amero, Khaled K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Saudi Medical Journal 2015
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362195/
https://www.ncbi.nlm.nih.gov/pubmed/25630015
http://dx.doi.org/10.15537/smj.2015.1.9697

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362195/
https://www.ncbi.nlm.nih.gov/pubmed/25630015
http://dx.doi.org/10.15537/smj.2015.1.9697

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