Three Novel Mutations in CYP21 Gene in Brazilian Patients with the Classical Form of 21-Hydroxylase Deficiency Due to a Founder Effect

✍ Scribed by Billerbeck, Ana Elisa C.; Mendonca, Berenice B.; Pinto, Emilia M.; Madureira, Guiomar; Arnhold, Ivo J. P.; Bachega, Tânia A. S. S.

• Book ID: 124081599
• Publisher: Endocrine Society
• Year: 2002
• Tongue: English
• Weight: 87 KB
• Volume: 87
• Category: Article
• ISSN: 0021-972X
• DOI: 10.1210/jc.2001-011939