A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Authors:
- Wendy TurattiWTWendy Turatti
- Paula Conde Lamparelli EliasPEPaula Conde Lamparelli Elias
- Lucila Leico Kagohara EliasLELucila Leico Kagohara Elias
- Carlos Eduardo MartinelliCMCarlos Eduardo Martinelli
- Ayrton Custodio MoreiraAMAyrton Custodio Moreira
- Sonir Roberto AntoniniSASonir Roberto Antonini
- Margaret de CastroMCMargaret de Castro
Abstract
No abstract availableKeywords
Funding Information
- FAPESP (07/58365-3)
- CNPq (150648/2010-3, 500199/2010-8)
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