Functional analysis of two rare CYP21A2 mutations detected in Italian patients with a mildest form of congenital adrenal hyperplasia
Paola Concolino, Francesca Vendittelli, Enrica Mello, Angelo Minucci, Cinzia Carrozza, Aurora Rossodivita, Bruno Giardina, Cecilia Zuppi, Ettore CapoluongoVolume:
71
Year:
2009
Language:
english
Pages:
7
DOI:
10.1111/j.1365-2265.2008.03517.x
File:
PDF, 248 KB
english, 2009