17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene
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R. Schild | J. Grötzinger | S. Heger | M. Hartmann | S. Wudy | P. Holterhus | M. Welzel | F. Riepe | A. Kulle | Christina Petri | Jens Siegel