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Isolated 17,20-lyase deficiency due to the cytochrome b5 mutation W27X

Renée C Kok1, Marianna A Timmerman, Katja P Wolffenbuttel

  • 1Endocrine Laboratory, Department of Internal Medicine, Erasmus Medical Centre, P.O. Box 2040, 3000 CA Rotterdam, The Netherlands.

The Journal of Clinical Endocrinology and Metabolism
|January 19, 2010
PubMed
Abstract

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