A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

✍ Scribed by Coeli-Lacchini, Fernanda Borchers; Turatti, Wendy; Elias, Paula Conde Lamparelli; Elias, Lucila Leico Kagohara; Martinelli, Carlos Eduardo; Moreira, Ayrton Custodio; Antonini, Sonir Roberto; de Castro, Margaret

• Book ID: 120435955
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 949 KB
• Volume: 526
• Category: Article
• ISSN: 0378-1119
• DOI: 10.1016/j.gene.2013.03.082