Abstract
The laboratory of Human Molecular Genetics at CBMEG-UNICAMP in association with the Pediatric Endocrinology group at the Department of Pediatrics - FCM and also with the Department of Endocrinology at the FMRP-USP, is developing a research on mutation identification and characterization in the CYP21A2 gene responsible for Congenital Adrenal Hiperplasia (CAH) due to 21-hydroxylase deficien…