Menabo, S. Et Al. 2014. Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.22, no.5 , 610-616.

Menabo, S., Polat, S., Baldazzi, L., Kulle, A. E., Holterhus, P., Groetzinger, J., ... Fanelli, F.(2014). Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.22, no.5, 610-616.

Menabo, Soara Et Al. "Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.22, no.5, 610-616, 2014

Menabo, Soara Et Al. "Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.22, no.5, pp.610-616, 2014

Menabo, S. Et Al. (2014) . "Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.22, no.5, pp.610-616.

@article{article, author={Soara Menabo Et Al. }, title={Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2014, pages={610-616} }