Clinical, Genetic and Functional Characteristics of Three Novel CYP17A1 Mutations Causing Combined 17α-Hydroxylase/17,20-Lyase Deficiency

Publisher： Karger

E-ISSN： 1663-2826|73|3|198-204

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.73, Iss.3, 2010-03, pp. : 198-204

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