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

Autor: Ben Charfeddine, Ilhem, Riepe, Felix G., Kahloul, Najoua, Kulle, Alexandra E., Adala, Labiba, Mamaï, Ons, Amara, Abdelbasset, Mili, Amira, Amri, Fathi, Saad, Ali, Holterhus, Paul-Martin, Gribaa, Moez
Zdroj: In General and Comparative Endocrinology 2012 175(3):514-518
Databáze: ScienceDirect
Externí odkaz: