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bibliographicCitation Laflamme N, Leblanc JF, Mailloux J, Faure N, Labrie F, Simard J. Mutation R96W in cytochrome P450c17 gene causes combined 17 alpha-hydroxylase/17-20-lyase deficiency in two French Canadian patients. The Journal of Clinical Endocrinology & Metabolism. 1996 Jan;81(1):264–8. doi: 10.1210/jcem.81.1.8550762.
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title Mutation R96W in cytochrome P450c17 gene causes combined 17 alpha-hydroxylase/17-20-lyase deficiency in two French Canadian patients.
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