Linkage between I172N mutation, a marker of 21-hydroxylase deficiency, and a single nucleotide polymorphism in Int6 of CYP21B gene: A genetic study of Sardinian family

✍ Scribed by Paola Concolino; Maria Antonia Satta; Concetta Santonocito; Cinzia Carrozza; Sandro Rocchetti; Franco Ameglio; Emiliano Giardina; Cecilia Zuppi; Ettore Capoluongo

• Book ID: 116346944
• Publisher: Elsevier Science
• Year: 2006
• Tongue: English
• Weight: 246 KB
• Volume: 364
• Category: Article
• ISSN: 0009-8981
• DOI: 10.1016/j.cca.2005.07.020