17a-Hydroxylase Deficiency Diagnosed in Early Infancy...

Hormone Research in Paediatrics 2014 Vol. 81; Iss. 5

17a-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene

Petri, Christina, Wudy, Stefan A., Riepe, Felix G., Holterhus, Paul-Martin, Siegel, Jens, Hartmann, Michaela F., Kulle, Alexandra E., Welzel, Maik, Grötzinger, Joachim, Schild, Ralf L., Heger, Sabine
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Volume:
81
Year:
2014
Language:
english
Journal:
Hormone Research in Paediatrics
DOI:
10.1159/000357065
File:
PDF, 506 KB
english, 2014
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