Mutation spectrum ofCYP21A2and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency

✍ Scribed by Dung, Vu; Khanh, Tran; Fukami, Maki; Phuong, Le; Ha, Nguyen; Liem, Nguyen; Van, Ta

• Book ID: 121617277
• Publisher: BioMed Central
• Year: 2013
• Tongue: English
• Weight: 337 KB
• Volume: 2013
• Category: Article
• ISSN: 1687-9848
• DOI: 10.1186/1687-9856-2013-S1-P128