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CYP21A2 Gene Mutations in Congenital Adrenal Hyperplasia: Genotype−phenotype correlation in Turkish children

Background: Congenital adrenal hyperplasia (CAH) due 21−hydroxylase deficiency (21−OHD) is a common autosomal recessive disorder. It is caused by defects in the CYP21A2 gene. Objective: Our aim was to determine the frequency of common gene mutations and to evaluate genotype−phenotype correlations in...

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Detalles Bibliográficos
Autores principales:	Baş, Firdevs, Kayserili, Hülya, Darendeliler, Feyza, Uyguner, Oya, Günöz, Hülya, Yüksel Apak, Memnune, Atalar, Fatmahan, Bundak, Rüveyde, Wilson, Robert C., New, Maria I., Wollnik, Bernd, Saka, Nurçin
Formato:	Texto
Lenguaje:	English
Publicado:	Galenos Publishing 2009
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005650/ https://www.ncbi.nlm.nih.gov/pubmed/21274396 http://dx.doi.org/10.4008/jcrpe.v1i3.49

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