Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene

Congenital adrenal hyperplasia (CAH) is characterized by impaired biosynthesis of cortisol. 21-hydroxylase deficiency is the most common cause of CAH affecting 1 in 10000-15000 live births over the world. The frequency of the disorder is very high in Iran due to frequent consanguineous marriages. Al...

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Detalles Bibliográficos
Autores principales: Rabbani, Bahareh, Mahdieh, Nejat, Haghi Ashtiani, Mohammad-Taghi, Akbari, Mohammad-Taghi, Rabbani, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2011
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446151/
https://www.ncbi.nlm.nih.gov/pubmed/23056780

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446151/
https://www.ncbi.nlm.nih.gov/pubmed/23056780

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