Opening book details…
About this Medicine article
High frequency of Q318X mutation in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in northeast Brazil by Campos, Viviane C.; Pereira, Rossana M. C.; Torres, Natália; Castro, Margaret de; Aguiar-Oliveira, Manuel H. is a Medicine article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Medicine.
- Author
- Campos, Viviane C.; Pereira, Rossana M. C.; Torres, Natália; Castro, Margaret de; Aguiar-Oliveira, Manuel H.
- Publisher
- SciELO; Universidade de Sao Paulo; FapUNIFESP (SciELO); São Paulo SP: Sociedade Brasileira de Endocrinologia e Metabologia (ISSN 0004-2730)
- Published
- 2009
- Language
- EN
- Field
- Medicine (Health Sciences)