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New Mutation Of CYP24A1 In A Case Of Idiopathic Infantile Hypercalcemia Diagnosed In Adulthood
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New mutation of cyp24a1 in a case of idiopathic infantile hypercalcemia.

Figure 1 from a case of idiopathic infantile hypercalcemia with severe.

Successful treatment of hypercalcemia in a chinese patient with a novel.