Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family

✍ Scribed by Ilhem Ben Charfeddine; Felix G. Riepe; Najoua Kahloul; Alexandra E. Kulle; Labiba Adala; Ons Mamaï; Abdelbasset Amara; Amira Mili; Fathi Amri; Ali Saad; Paul-Martin Holterhus; Moez Gribaa

• Book ID: 113958846
• Publisher: Elsevier Science
• Year: 2012
• Tongue: English
• Weight: 807 KB
• Volume: 175
• Category: Article
• ISSN: 0016-6480
• DOI: 10.1016/j.ygcen.2011.12.017