Ethnic disparity in 21-hydroxylase gene mutations identified in Pakistani congenital adrenal hyperplasia patients

BACKGROUND: Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders caused by defects in the steroid 21 hydroxylase gene (CYP21A2). We studied the spectrum of mutations in CYP21A2 gene in a multi-ethnic population in Pakistan to explore the genetics of CAH. METHODS: A cross...

Descrición completa

Gardado en:
Detalles Bibliográficos
Main Authors: Khan, Aysha H, Aban, Muniba, Raza, Jamal, ul Haq, Naeem, Jabbar, Abdul, Moatter, Tariq
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2011
Assuntos:
Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3050769/
https://ncbi.nlm.nih.gov/pubmed/21329531
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1472-6823-11-5
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares