A New Compound Heterozygous Mutation (W17X, 436+5G->T) in the Cytochrome P450c17 Gene Causes 17 -Hydroxylase/17,20-Lyase Deficiency
- 1 January 1998
- journal article
- Published by The Endocrine Society in Journal of Clinical Endocrinology & Metabolism
- Vol. 83 (1) , 199-202
- https://doi.org/10.1210/jc.83.1.199
Abstract
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