Heterozygosis for CYP21A2 mutation considered as 21-hydroxylase deficiency in neonatal screening

by Soardi,Fernanda Caroline, Lemos-Marini,Sofia Helena V., Coeli,Fernanda Borchers, Maturana,Víctor Gonçalves, Silva,Márcia Duarte Barbosa da, Bernardi,Renan Darin, Justo,Giselle Zenker, de-Mello,Maricilda Palandi
Published 2008