Functional analysis of two rare CYP21A2 mutations detected in Italian patients with a mildest form of congenital adrenal hyperplasia

Cinzia Carrozza, Paola Concolino, Francesca Vendittelli, Angelo Minucci, Aurora Natalia Rossodivita, Bruno Giardina, Cecilia Zuppi, Ettore Domenico Capoluongo, E Mello

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Medicine & Life Sciences