Three Novel CYP11B1 Mutations in Congenital Adrenal Hyperplasia due to Steroid 11Beta-Hydroxylase Deficiency in a Moroccan Population

Publisher： Karger

E-ISSN： 1663-2826|74|3|182-189

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.74, Iss.3, 2010-06, pp. : 182-189

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Over 50 Years of Progress in the Treatment of the Hypertensive Form of Congenital Adrenal Hyperplasia due to Steroid 11-Beta-Hydroxylase Deficiency

By  

Hormone Research in Paediatrics, Vol. 68, Iss. 6, 2007-08 ,pp. : 298-299

Karger

Access to resources Recommend Favorite

Congenital Adrenal Hyperplasia due to 11-Hydroxylase Deficiency – Insights from Two Novel CYP11B1 Mutations (p.M92X, p.R453Q)

By  

Hormone Research in Paediatrics, Vol. 72, Iss. 5, 2009-10 ,pp. : 281-286

Karger

Access to resources Recommend Favorite

Successful Pregnancy in a Patient with Severe 11-Beta-Hydroxylase Deficiency and Novel Mutations in CYP11B1 Gene

By  

Hormone Research in Paediatrics, Vol. 68, Iss. 6, 2007-08 ,pp. : 294-297

Karger

Access to resources Recommend Favorite

Steroid 11-Beta-Hydroxylase Deficiency Caused by Compound Heterozygosity for a Novel Mutation, p.G314R, in One CYP11B1 Allele, and a Chimeric CYP11B2/CYP11B1 in the Other Allele

By  

Hormone Research in Paediatrics, Vol. 63, Iss. 6, 2005-08 ,pp. : 284-293

Karger

Access to resources Recommend Favorite

A Homozygous L299P Mutation in the CYP11B1 Gene Leads to Complete Virilization in 46,XX Individuals with 11-Beta-Hydroxylase Deficiency

By  

Hormone Research in Paediatrics, Vol. 70, Iss. 3, 2008-07 ,pp. : 145-149

Karger

Access to resources Recommend Favorite