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Thats not how we should treat people who want to go on these medications, says Kai Jones, an endocrinologist at Washington University in St
Several small-molecule inhibitors of CYP51A1 have been developed, including clinically used azoles such as fluconazole and ketoconazole, which were originally designed to target fungal CYP51A1 but also inhibit the human enzyme (Table 3)
The protocol needs to be sustainable for a year or more
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