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CYP24A1 and SLC34A1 genetic defects associated with idiopathic infantile hypercalcemia: from genotype to phenotype
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Figure 1 from CYP3A4 Induction by Rifampin: An Alternative Pathway for Vitamin D Inactivation in Patients With CYP24A1 Mutations | Semantic Scholar
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Regulation of expression of CYP27B1 and CYP24A1 by 1α,25(OH) 2 D, PTH,... | Download Scientific Diagram
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Intractable hypercalcaemia during pregnancy and the postpartum secondary to pathogenic variants in CYP24A1 in: Endocrinology, Diabetes & Metabolism Case Reports Volume 2019 Issue 1 (2019)
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Major causes of high CYP24A1 expression. Besides VD metabolites, other... | Download Scientific Diagram
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A CYP24A1 Gene Mutation: A Rare Cause of Adult Onset Recurrent Nephrolithiasis | Journal of Case Reports in Medicine
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