Molecular genetic analysis of CYP21A2 gene in patients with congenital adrenal hyperplasia

CONTEXT: Congenital adrenal hyperplasia (CAH) is one of the inborn errors of metabolic disorder inherited in an autosomal recessive manner caused by the defects in the steroid 21 hydroxylase CYP21A2 gene. We analyzed the genotype of 62 patients with classic CAH. AIMS: To find out the underlying muta...

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Detalles Bibliográficos
Autores principales: Marumudi, Eunice, Sharma, Arundhati, Kulshreshtha, Bindu, Khadgawat, Rajesh, Khurana, Madan L., Ammini, Ariachery C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354845/
https://www.ncbi.nlm.nih.gov/pubmed/22629504
http://dx.doi.org/10.4103/2230-8210.95679

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354845/
https://www.ncbi.nlm.nih.gov/pubmed/22629504
http://dx.doi.org/10.4103/2230-8210.95679

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