Steroid 11-Beta-Hydroxylase Deficiency Caused by Compound Heterozygosity for a Novel Mutation, p.G314R, in One CYP11B1 Allele, and a Chimeric CYP11B2/CYP11B1 in the Other Allele

Publisher： Karger

E-ISSN： 1663-2826|63|6|284-293

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.63, Iss.6, 2005-08, pp. : 284-293

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