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Combined 17α-hydroxylase/17,20-lyase deficiency due to p.R96W mutation in the CYP17 gene in a Brazilian patient

Overview of attention for article published in Archives of Endocrinology and Metabolism, February 2011
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Title
Combined 17α-hydroxylase/17,20-lyase deficiency due to p.R96W mutation in the CYP17 gene in a Brazilian patient
Published in
Archives of Endocrinology and Metabolism, February 2011
DOI 10.1590/s0004-27302010000800014
Pubmed ID
Authors

Fabíola Costenaro, Ticiana C. Rodrigues, Claudio E. Kater, Richard J. Auchus, Mahboubeh Papari-Zareei, Mauro A. Czepielewski